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79-07-2

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79-07-2 Usage

Description

Chloroacetamide is a preservative used in several applications such as in cutting metalwork fluids, in paints or in glues. It can induce contact dermatitis in hairdressers, or in shoemakers when used as a leather preservative.

Chemical Properties

white crystalline powder

Uses

Different sources of media describe the Uses of 79-07-2 differently. You can refer to the following data:
1. A component of herbicidal mixtures of cellulose biosynthesis inhibitors with VLCFA inhibitors.
2. 2-Chloroacetamide is used as surface-active agent in home laundry, cleaning products & household formulated cleaners, other industrial uses, petroleum production, polymer processing.
3. preservative in cosmetic and pharmaceutical creams, shampoos, bath lotions, etc.; preservative in glues, cooling fluids.

Flammability and Explosibility

Nonflammable

Contact allergens

Chloroacetamide as a preservative is used in several applications as in cutting metalworking fluids, in paints or in glues. It can induce contact dermatitis in hairdressers or in shoemakers, being used as a leather preservative.

Safety Profile

Poison by ingestion, intravenous, and intraperitoneal routes. Mutation data reported. When heated to decomposition it emits very toxic Cland NOx. See also N-CHLOROACETAMIDE.

Purification Methods

Recrystallise the amide from acetone and dry it under vacuum over P2O5. [Beilstein 2 IV 490.]

Check Digit Verification of cas no

The CAS Registry Mumber 79-07-2 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79-07:
(4*7)+(3*9)+(2*0)+(1*7)=62
62 % 10 = 2
So 79-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H4ClNO/c3-1-2(4)5/h1H2,(H2,4,5)

79-07-2 Well-known Company Product Price

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  • Alfa Aesar

  • (A15238)  2-Chloroacetamide, 98+%   

  • 79-07-2

  • 250g

  • 297.0CNY

  • Detail
  • Alfa Aesar

  • (A15238)  2-Chloroacetamide, 98+%   

  • 79-07-2

  • 1000g

  • 679.0CNY

  • Detail
  • Alfa Aesar

  • (A15238)  2-Chloroacetamide, 98+%   

  • 79-07-2

  • 5000g

  • 2844.0CNY

  • Detail

79-07-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Chloroacetamide

1.2 Other means of identification

Product number -
Other names Acetamide, 2-chloro-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79-07-2 SDS

79-07-2Synthetic route

1-dodecene
112-41-4

1-dodecene

N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

A

2-Chloro-N-(2-chloro-dodecyl)-acetamide
35077-34-0

2-Chloro-N-(2-chloro-dodecyl)-acetamide

B

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; Irradiation;A 95%
B 3%
tert-butyl (2-chloroacetyl)carbamate
120158-03-4

tert-butyl (2-chloroacetyl)carbamate

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With trifluoroacetic acid In dichloromethane for 1h; Ambient temperature;94%
N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With n-octyne In dichloromethane at 15 - 20℃; Irradiation;93%
chloroacetonitrile
107-14-2

chloroacetonitrile

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With Amberlyst A-26 (OH- form); dihydrogen peroxide In methanol at 20℃; for 2h; Hydrolysis;93%
With [RuCl2(η6-p-cymene)(P(4-C6H4F)2Cl)]; water at 40℃; for 1h; Sealed tube; Inert atmosphere;93%
With C19H23Cl2N6PRuS3*3ClH; water at 100℃; for 1h; Inert atmosphere; Schlenk technique;88%
α-chloro-N-bromoacetamide
35077-11-3

α-chloro-N-bromoacetamide

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With 1,2-dimethylcyclohexene In dichloromethane at 15 - 20℃; Irradiation;92%
With perchloric acid; water; potassium hydrogen phthalate; potassium nitrate; potassium bromide at 25℃; for 1h; Equilibrium constant;
1-methylcyclohex-1-ene
591-49-1

1-methylcyclohex-1-ene

N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

2-Chloro-N-((1S,2R)-2-chloro-2-methyl-cyclohexyl)-acetamide
35077-36-2, 64226-98-8

2-Chloro-N-((1S,2R)-2-chloro-2-methyl-cyclohexyl)-acetamide

B

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; Irradiation;A 88%
B 7%
methanol
67-56-1

methanol

methyl 2-chloroacetimidate hydrochloride
70737-12-1

methyl 2-chloroacetimidate hydrochloride

A

2-chloro-1,1,1-trimethoxyethane
74974-54-2

2-chloro-1,1,1-trimethoxyethane

B

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
at 20℃; for 24h;A 65%
B n/a
1-dodecene
112-41-4

1-dodecene

α-chloro-N-bromoacetamide
35077-11-3

α-chloro-N-bromoacetamide

A

N-(2-Bromo-dodecyl)-2-chloro-acetamide
35077-35-1

N-(2-Bromo-dodecyl)-2-chloro-acetamide

B

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; Irradiation;A 62%
B 30%
N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

1-chlorocyclohexene
930-66-5

1-chlorocyclohexene

A

2-Chloro-N-(2,2-dichloro-cyclohexyl)-acetamide
78174-21-7

2-Chloro-N-(2,2-dichloro-cyclohexyl)-acetamide

B

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; Irradiation;A 35%
B 59%
N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

1-cyclohexenyl methyl ketone
932-66-1

1-cyclohexenyl methyl ketone

N-((1S,2R)-2-Acetyl-2-chloro-cyclohexyl)-2-chloro-acetamide
35077-39-5, 35077-40-8

N-((1S,2R)-2-Acetyl-2-chloro-cyclohexyl)-2-chloro-acetamide

N-((1R,2R)-2-Acetyl-2-chloro-cyclohexyl)-2-chloro-acetamide
35077-39-5, 35077-40-8

N-((1R,2R)-2-Acetyl-2-chloro-cyclohexyl)-2-chloro-acetamide

C

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; Irradiation;A 16%
B 54%
C 30%
1-methylcyclohex-1-ene
591-49-1

1-methylcyclohex-1-ene

α-chloro-N-bromoacetamide
35077-11-3

α-chloro-N-bromoacetamide

N-((1S,2R)-2-Bromo-2-methyl-cyclohexyl)-2-chloro-acetamide
35077-37-3, 35077-38-4

N-((1S,2R)-2-Bromo-2-methyl-cyclohexyl)-2-chloro-acetamide

N-((1R,2R)-2-Bromo-2-methyl-cyclohexyl)-2-chloro-acetamide
35077-37-3, 35077-38-4

N-((1R,2R)-2-Bromo-2-methyl-cyclohexyl)-2-chloro-acetamide

C

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; Irradiation;A 48%
B 14%
C 35%
α-chloro-N-bromoacetamide
35077-11-3

α-chloro-N-bromoacetamide

cyclohexene
110-83-8

cyclohexene

N-((1S,2R)-2-Bromo-cyclohexyl)-2-chloro-acetamide
35077-28-2, 35077-29-3

N-((1S,2R)-2-Bromo-cyclohexyl)-2-chloro-acetamide

N-(trans-2-bromocyclohexyl)chloroacetamide
35077-28-2, 35077-29-3

N-(trans-2-bromocyclohexyl)chloroacetamide

C

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; for 1.5h; Irradiation; Yield given. Yields of byproduct given;A n/a
B n/a
C 37%
methanol
67-56-1

methanol

cyclohexene
110-83-8

cyclohexene

trans-3-bromomethoxycyclohexane

trans-3-bromomethoxycyclohexane

N-((1S,2R)-2-Bromo-cyclohexyl)-2-chloro-acetamide
35077-28-2, 35077-29-3

N-((1S,2R)-2-Bromo-cyclohexyl)-2-chloro-acetamide

N-(trans-2-bromocyclohexyl)chloroacetamide
35077-28-2, 35077-29-3

N-(trans-2-bromocyclohexyl)chloroacetamide

D

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With α-chloro-N-bromoacetamide at -70℃; for 17h; Irradiation; Yields of byproduct given;A 27%
B n/a
C n/a
D 31%
norborn-2-ene
498-66-8

norborn-2-ene

α-chloro-N-bromoacetamide
35077-11-3

α-chloro-N-bromoacetamide

N-((1R,2S,3S,4S)-3-Bromo-bicyclo[2.2.1]hept-2-yl)-2-chloro-acetamide
64227-10-7, 64312-52-3

N-((1R,2S,3S,4S)-3-Bromo-bicyclo[2.2.1]hept-2-yl)-2-chloro-acetamide

N-((1R,2S,3R,4S)-3-Bromo-bicyclo[2.2.1]hept-2-yl)-2-chloro-acetamide
64227-10-7, 64312-52-3

N-((1R,2S,3R,4S)-3-Bromo-bicyclo[2.2.1]hept-2-yl)-2-chloro-acetamide

C

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; Irradiation; Yield given. Yields of byproduct given;A n/a
B n/a
C 30%
N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

cyclohexene
110-83-8

cyclohexene

N-(trans-2-chlorocyclohexyl)acetamide
24281-07-0, 33092-85-2, 35077-14-6, 53297-75-9

N-(trans-2-chlorocyclohexyl)acetamide

2-Chloro-N-((1S,2R)-2-chloro-cyclohexyl)-acetamide
35077-18-0, 35077-19-1

2-Chloro-N-((1S,2R)-2-chloro-cyclohexyl)-acetamide

2-Chloro-N-((1S,2S)-2-chloro-cyclohexyl)-acetamide
35077-18-0, 35077-19-1

2-Chloro-N-((1S,2S)-2-chloro-cyclohexyl)-acetamide

D

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In acetonitrile at 15 - 20℃; Irradiation; Yields of byproduct given;A 18%
B n/a
C n/a
D 12%
norborn-2-ene
498-66-8

norborn-2-ene

N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

2-Chloro-N-((1R,2S,3S,4S)-3-chloro-bicyclo[2.2.1]hept-2-yl)-acetamide
64227-07-2, 64281-95-4

2-Chloro-N-((1R,2S,3S,4S)-3-chloro-bicyclo[2.2.1]hept-2-yl)-acetamide

2-Chloro-N-((1R,2S,3R,4S)-3-chloro-bicyclo[2.2.1]hept-2-yl)-acetamide
64227-07-2, 64281-95-4

2-Chloro-N-((1R,2S,3R,4S)-3-chloro-bicyclo[2.2.1]hept-2-yl)-acetamide

C

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; Irradiation; Yield given. Yields of byproduct given;A n/a
B n/a
C 10%
N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

cyclohexene
110-83-8

cyclohexene

2-Chloro-N-((1S,2R)-2-chloro-cyclohexyl)-acetamide
35077-18-0, 35077-19-1

2-Chloro-N-((1S,2R)-2-chloro-cyclohexyl)-acetamide

2-Chloro-N-((1S,2S)-2-chloro-cyclohexyl)-acetamide
35077-18-0, 35077-19-1

2-Chloro-N-((1S,2S)-2-chloro-cyclohexyl)-acetamide

C

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
In dichloromethane at 15 - 20℃; for 2.5h; Irradiation; Yield given;A n/a
B n/a
C 9%
Ketene
463-51-4

Ketene

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With nitrogen trichloride; diethyl ether at -60℃; unter Ausschluss von Feuchtigkeit;
ethanol
64-17-5

ethanol

dichlorodiacetamide
4960-82-1

dichlorodiacetamide

A

chloroacetic acid ethyl ester
105-39-5

chloroacetic acid ethyl ester

B

Chloroacetamide
79-07-2

Chloroacetamide

methyl chloroacetate
96-34-4

methyl chloroacetate

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With ammonia; water
sodium methylate In methanol
sodium methylate In methanol
chloroacetic acid ethyl ester
105-39-5

chloroacetic acid ethyl ester

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With ammonia
With ammonium hydroxide
With ammonium hydroxide
With ammonium hydroxide at 0℃;
With ammonium hydroxide at 0℃; for 0.25h; Temperature;
chloroacetic acid
79-11-8

chloroacetic acid

urea
57-13-6

urea

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
at 160 - 170℃;
chloroacetyl chloride
79-04-9

chloroacetyl chloride

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With ammonia
With sulfuric acid; 1,1,1,3,3,3-hexamethyl-disilazane 1.) CH2Cl2, room temp., 2.) CH3OH; Yield given. Multistep reaction;
With ammonia; triethylamine In chloroform at 20℃; for 2h; Substitution;
2-aminopyridine
504-29-0

2-aminopyridine

2-Chloro-N-(1λ5-pyrrolidin-1-ylidenemethyl)-acetamide

2-Chloro-N-(1λ5-pyrrolidin-1-ylidenemethyl)-acetamide

A

N-(2-Pyridino)-N,N'-tetramethylenformamidin

N-(2-Pyridino)-N,N'-tetramethylenformamidin

B

Chloroacetamide
79-07-2

Chloroacetamide

N-chloro-alpha-chloroacetamide
35070-77-0

N-chloro-alpha-chloroacetamide

2-Chloro-N-(2,2-dimethoxy-cyclohexyl)-acetamide
78174-28-4

2-Chloro-N-(2,2-dimethoxy-cyclohexyl)-acetamide

A

α-chloroacetamidocyclohexanone
35077-41-9

α-chloroacetamidocyclohexanone

B

2-Chlorocyclohexanone
822-87-7

2-Chlorocyclohexanone

C

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With water -70 degC, then allowed to warm to r.t.; Yield given. Yields of byproduct given;
1-methoxy-cyclohex-1-ene
931-57-7

1-methoxy-cyclohex-1-ene

A

2-bromocyclohexanone
1056477-06-5

2-bromocyclohexanone

B

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
Yield given. Multistep reaction. Yields of byproduct given;
(1-methoxyethylidene)cyclohexane
26473-57-4

(1-methoxyethylidene)cyclohexane

A

1-(1-chlorocyclohexyl)ethanone
1004-55-3

1-(1-chlorocyclohexyl)ethanone

B

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With N-chloro-alpha-chloroacetamide; water 1.) irradiation, CH2Cl2; Yield given. Multistep reaction. Yields of byproduct given;
chloro-acetic acid benzhydrylidenamide
36709-55-4

chloro-acetic acid benzhydrylidenamide

A

benzophenone
119-61-9

benzophenone

B

Chloroacetamide
79-07-2

Chloroacetamide

Conditions
ConditionsYield
With water at 25℃; Rate constant; effect of pH on the rate constants;
potassium cyanamide salt
29422-34-2

potassium cyanamide salt

Chloroacetamide
79-07-2

Chloroacetamide

C6H9N3O2S

C6H9N3O2S

Conditions
ConditionsYield
In acetone for 1h; Ambient temperature;100%
6-mercapto-3,3-dimethyl-8-dimethylamino-3,4-dihydro-1H-pyrano[3,4-c]-pyridine-5-carbonitrile
889656-79-5

6-mercapto-3,3-dimethyl-8-dimethylamino-3,4-dihydro-1H-pyrano[3,4-c]-pyridine-5-carbonitrile

Chloroacetamide
79-07-2

Chloroacetamide

1-amino-5-dimethylamino-8,8-dimethyl-8,9-dihydro-6H-pyrano[4,3-d]thieno[2,3-b]pyridine-2-carboxamide
889656-80-8

1-amino-5-dimethylamino-8,8-dimethyl-8,9-dihydro-6H-pyrano[4,3-d]thieno[2,3-b]pyridine-2-carboxamide

Conditions
ConditionsYield
With potassium carbonate In ethanol at 20℃; for 5h; Heating / reflux;100%
With potassium carbonate In ethanol for 4h; Reflux; Inert atmosphere;
1-(benzylmethylamino)-3-mercapto-6,6-dimethyl-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile
890023-58-2

1-(benzylmethylamino)-3-mercapto-6,6-dimethyl-5,6,7,8-tetrahydro-isoquinoline-4-carbonitrile

Chloroacetamide
79-07-2

Chloroacetamide

C22H26N4OS
890023-59-3

C22H26N4OS

Conditions
ConditionsYield
With potassium carbonate In ethanol Heating / reflux;100%
With potassium carbonate In ethanol for 4h; Reflux; Inert atmosphere;
glyoxylic acid ethyl ester
924-44-7

glyoxylic acid ethyl ester

Chloroacetamide
79-07-2

Chloroacetamide

ethyl 2-(2-chloroacetamido)-2-hydroxyacetate
1198115-96-6

ethyl 2-(2-chloroacetamido)-2-hydroxyacetate

Conditions
ConditionsYield
In tetrahydrofuran; toluene at 80℃; Inert atmosphere;100%
4-nitro-1H-pyrazole
2075-46-9

4-nitro-1H-pyrazole

Chloroacetamide
79-07-2

Chloroacetamide

2-(4-nitro-1H-pyrazol-1-yl)acetamide
32407-64-0

2-(4-nitro-1H-pyrazol-1-yl)acetamide

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 60℃;100%
2-nitro-benzaldehyde
552-89-6

2-nitro-benzaldehyde

Chloroacetamide
79-07-2

Chloroacetamide

trans-3-(2-nitrophenyl)oxirane-2-carboxamide
109287-33-4

trans-3-(2-nitrophenyl)oxirane-2-carboxamide

Conditions
ConditionsYield
With sodium ethanolate In ethanol at 20℃; for 7h; Darzens Condensation; stereoselective reaction;100%
With sodium ethanolate In ethanol at 20℃; for 5h;100%
triphenylphosphine
603-35-0

triphenylphosphine

Chloroacetamide
79-07-2

Chloroacetamide

(2-amino-2-oxo-ethyl)triphenyl-phosphonium chloride
25361-54-0

(2-amino-2-oxo-ethyl)triphenyl-phosphonium chloride

Conditions
ConditionsYield
In nitromethane at 105℃; for 19h; Schlenk technique;99%
In nitromethane at 105℃; for 19h; Inert atmosphere;98%
In acetonitrile for 11h; Heating; Inert atmosphere;96%
In various solvent(s) at 100℃; for 16h;84%
4-hydroxy-benzaldehyde
123-08-0

4-hydroxy-benzaldehyde

Chloroacetamide
79-07-2

Chloroacetamide

2-(4-formyl-phenoxy)-acetamide
135857-20-4

2-(4-formyl-phenoxy)-acetamide

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In acetone for 48h; Reflux;99%
With potassium carbonate In N,N-dimethyl-formamide at 110℃; for 2h;
With potassium carbonate In acetonitrile Reflux;
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 20℃; for 5h;
3-mercapto-1-dimethylamino-6,6-dimethyl-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile
890023-03-7

3-mercapto-1-dimethylamino-6,6-dimethyl-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile

Chloroacetamide
79-07-2

Chloroacetamide

1-amino-5-dimethylamino-8,8-dimethyl-6,7,8,9-tetrahydrothieno[2,3-c]isoquinoline-2-carboxamide
890023-04-8

1-amino-5-dimethylamino-8,8-dimethyl-6,7,8,9-tetrahydrothieno[2,3-c]isoquinoline-2-carboxamide

Conditions
ConditionsYield
With potassium carbonate In ethanol Heating / reflux;99%
1-dimethylamino-3-mercapto-6,6-dimethyl-6,7-dihydro-5H-[2]pyridin-4-carbonitrile
890023-33-3

1-dimethylamino-3-mercapto-6,6-dimethyl-6,7-dihydro-5H-[2]pyridin-4-carbonitrile

Chloroacetamide
79-07-2

Chloroacetamide

1-amino-5-dimethylamino-7,7-dimethyl-6H-7,8-dihydrocycIopenta[d]thieno[2,3-b]pyridin-2-carboxamide
890023-34-4

1-amino-5-dimethylamino-7,7-dimethyl-6H-7,8-dihydrocycIopenta[d]thieno[2,3-b]pyridin-2-carboxamide

Conditions
ConditionsYield
With potassium carbonate In ethanol Heating / reflux;99%
[2-[3-(3-fluoro-benzyloxy)-phenyl]-ethyl]-(furan-2-ylmethyl)amine
942302-89-8

[2-[3-(3-fluoro-benzyloxy)-phenyl]-ethyl]-(furan-2-ylmethyl)amine

Chloroacetamide
79-07-2

Chloroacetamide

2-[[2-[3-(3-fluoro-benzyloxy)-phenyl]-ethyl]-(furan-2-ylmethyl)amino]-acetamide

2-[[2-[3-(3-fluoro-benzyloxy)-phenyl]-ethyl]-(furan-2-ylmethyl)amino]-acetamide

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 120℃; for 2h; microwave irradiation;99%
4-Trifluoromethylbenzaldehyde
455-19-6

4-Trifluoromethylbenzaldehyde

Chloroacetamide
79-07-2

Chloroacetamide

2,3-epoxy-3-(4-trifluoromethylphenyl)propionamide

2,3-epoxy-3-(4-trifluoromethylphenyl)propionamide

Conditions
ConditionsYield
With sodium ethanolate In ethanol at 20℃; for 5h;99%
2-chloro-p-cresol
6640-27-3

2-chloro-p-cresol

Chloroacetamide
79-07-2

Chloroacetamide

2-(2-chloro-4-methylphenoxy)acetamide
1248651-95-7

2-(2-chloro-4-methylphenoxy)acetamide

Conditions
ConditionsYield
With potassium carbonate at 82℃; for 0.166667h; Solvent; Microwave irradiation;98.7%
salicylonitrile
611-20-1

salicylonitrile

Chloroacetamide
79-07-2

Chloroacetamide

2-(2-cyanophenoxy)acetamide
54802-12-9

2-(2-cyanophenoxy)acetamide

Conditions
ConditionsYield
With potassium carbonate In acetone at 56℃;98.5%
Stage #1: salicylonitrile With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 1h;
Stage #2: Chloroacetamide In N,N-dimethyl-formamide at 80℃; for 3h;
With potassium carbonate In N,N-dimethyl-formamide at 80℃;
5-chloro-7-methoxy-1H-pyrazolo[4,3-d]pyrimidine

5-chloro-7-methoxy-1H-pyrazolo[4,3-d]pyrimidine

Chloroacetamide
79-07-2

Chloroacetamide

A

2-(5-chloro-7-methoxy-1H-pyrazolo[4,3-d]pyrimidin-1-yl)acetamide

2-(5-chloro-7-methoxy-1H-pyrazolo[4,3-d]pyrimidin-1-yl)acetamide

B

2-(5-chloro-7-methoxypyrazolo[4,3-d]pyrimidin-2-yl)acetamide

2-(5-chloro-7-methoxypyrazolo[4,3-d]pyrimidin-2-yl)acetamide

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 70℃; for 10h;A 98.21%
B n/a
picoline
108-89-4

picoline

Chloroacetamide
79-07-2

Chloroacetamide

1-(2-amino-2-oxoethyl)-4-methylpyridinium chloride
78572-45-9

1-(2-amino-2-oxoethyl)-4-methylpyridinium chloride

Conditions
ConditionsYield
In acetonitrile at 80℃; for 48h;98%
In acetone at 25℃; for 72h;75%
In toluene for 5h; Reflux;52%
6-(4-chlorophenyl)-3-cyano-4-trifluoromethyl-2(1H)-pyridone
147381-62-2

6-(4-chlorophenyl)-3-cyano-4-trifluoromethyl-2(1H)-pyridone

Chloroacetamide
79-07-2

Chloroacetamide

2-[6-(4-Chloro-phenyl)-3-cyano-4-trifluoromethyl-pyridin-2-yloxy]-acetamide
155635-60-2

2-[6-(4-Chloro-phenyl)-3-cyano-4-trifluoromethyl-pyridin-2-yloxy]-acetamide

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In acetone at 60℃; for 6h;98%
N-(O,O'-diisopropylthiophosphoryl)thioacetamide
121221-00-9

N-(O,O'-diisopropylthiophosphoryl)thioacetamide

Chloroacetamide
79-07-2

Chloroacetamide

aminocarbonylmethyl N-isopropoxythiophosphorylacetimidothioate

aminocarbonylmethyl N-isopropoxythiophosphorylacetimidothioate

Conditions
ConditionsYield
With triethylamine In acetonitrile for 3h; Heating;98%
2-amino-6-sulfanyl-4-(thiophen-2-yl)pyridine-3,5-dicarbonitrile

2-amino-6-sulfanyl-4-(thiophen-2-yl)pyridine-3,5-dicarbonitrile

Chloroacetamide
79-07-2

Chloroacetamide

2-(6-amino-3,5-dicyano-4-thiophen-2-yl-pyridin-2-ylsulfanyl)-acetamide
136633-82-4

2-(6-amino-3,5-dicyano-4-thiophen-2-yl-pyridin-2-ylsulfanyl)-acetamide

Conditions
ConditionsYield
With triethylamine In acetone at 20℃; for 5h;98%
potassium trifluoro[(1E)-3-methoxyprop-1-en-1-yl]borate

potassium trifluoro[(1E)-3-methoxyprop-1-en-1-yl]borate

Chloroacetamide
79-07-2

Chloroacetamide

2-chloro-trans-N-(3-methoxy-propenyl)-acetamide
1238357-72-6

2-chloro-trans-N-(3-methoxy-propenyl)-acetamide

Conditions
ConditionsYield
With oxygen; copper diacetate In dichloromethane; dimethyl sulfoxide at 40℃; for 20h; Molecular sieve; diastereoselective reaction;98%
3-((8-(tert-butoxycarbonyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoic acid
1352948-27-6

3-((8-(tert-butoxycarbonyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoic acid

Chloroacetamide
79-07-2

Chloroacetamide

tert-butyl 3-(3-((2-amino-2-oxoethoxy)carbonyl)benzyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate
1352948-59-4

tert-butyl 3-(3-((2-amino-2-oxoethoxy)carbonyl)benzyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 65℃; for 18h;98%
o-Hydroxyethylbenzene
90-00-6

o-Hydroxyethylbenzene

Chloroacetamide
79-07-2

Chloroacetamide

2-(2-ethylphenoxy)acetamide
35368-61-7

2-(2-ethylphenoxy)acetamide

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In butanone for 48h; Reflux; Inert atmosphere;98%
5-(4-methoxybenzyl)-4-phenyl-4H-1,2,4-triazole-3-thiol
342597-54-0

5-(4-methoxybenzyl)-4-phenyl-4H-1,2,4-triazole-3-thiol

Chloroacetamide
79-07-2

Chloroacetamide

2-[5-(4-methoxybenzyl)-4-phenyl-4H-1,2,4-triazol-3-ylsulfanyl]acetamide
874798-09-1

2-[5-(4-methoxybenzyl)-4-phenyl-4H-1,2,4-triazol-3-ylsulfanyl]acetamide

Conditions
ConditionsYield
Stage #1: 5-(4-methoxybenzyl)-4-phenyl-4H-1,2,4-triazole-3-thiol With potassium hydroxide In ethanol Reflux;
Stage #2: Chloroacetamide In ethanol Reflux;
98%
6-hydroxy-2-pentyl-4-phenylquinoline-3-carbonitrile

6-hydroxy-2-pentyl-4-phenylquinoline-3-carbonitrile

Chloroacetamide
79-07-2

Chloroacetamide

2-((3-cyano-2-pentyl-4-phenylquinolin-6-yl)oxy)acetamide

2-((3-cyano-2-pentyl-4-phenylquinolin-6-yl)oxy)acetamide

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 12h;98%
5,5'-(octane-1,8-diyl)bis(4-allyl-4H-1,2,4-triazole-3-thiol)

5,5'-(octane-1,8-diyl)bis(4-allyl-4H-1,2,4-triazole-3-thiol)

Chloroacetamide
79-07-2

Chloroacetamide

2,2'-{octane-1,8-diylbis[(4-allyl-4H-1,2,4-triazole-3,5-diyl)sulfanediyl]}diacetamide

2,2'-{octane-1,8-diylbis[(4-allyl-4H-1,2,4-triazole-3,5-diyl)sulfanediyl]}diacetamide

Conditions
ConditionsYield
Heating;98%
diphenylchloromethane
90-99-3

diphenylchloromethane

Chloroacetamide
79-07-2

Chloroacetamide

2-(diphenylmethylthio)acetamide
68524-30-1

2-(diphenylmethylthio)acetamide

Conditions
ConditionsYield
Stage #1: diphenylchloromethane With thiourea; potassium iodide In water at 70 - 75℃; for 1.5h;
Stage #2: With sodium hydroxide In water at 15 - 24℃;
Stage #3: Chloroacetamide With triethylamine more than 3 stages;
97.9%
Stage #1: diphenylchloromethane With thiourea In isopropyl alcohol at 100℃; for 2h; Sealed tube;
Stage #2: Chloroacetamide With potassium hydroxide In methanol; isopropyl alcohol at 60℃; for 2h; Sonication;
Chloroacetamide
79-07-2

Chloroacetamide

α-chloro-N-bromoacetamide
35077-11-3

α-chloro-N-bromoacetamide

Conditions
ConditionsYield
With dibromoisocyanuric acid In dichloromethane for 5h; Bromination; Heating;97%
With perchloric acid; water; potassium hydrogen phthalate; potassium nitrate; potassium bromide at 25℃; for 1h; Equilibrium constant;
With bromine; trifluoroacetic acid; silver(l) oxide
With dibromoisocyanuric acid In dichloromethane
With sodium hypobromide
7-Amino<1,2,4>triazolo<1,5-c>pyrimidine-5(6H)-thione
70182-88-6

7-Amino<1,2,4>triazolo<1,5-c>pyrimidine-5(6H)-thione

Chloroacetamide
79-07-2

Chloroacetamide

(7-amino-s-triazole<1,5-c>pyrimidyl-5)thioacetic acid amide
143212-81-1

(7-amino-s-triazole<1,5-c>pyrimidyl-5)thioacetic acid amide

Conditions
ConditionsYield
With sodium ethanolate In ethanol for 3h; Heating;97%
Chloroacetamide
79-07-2

Chloroacetamide

acetamide
60-35-5

acetamide

Conditions
ConditionsYield
With borohydride exchange resin; nickel diacetate In methanol for 1h; Ambient temperature;97%
1,4-diaza-bicyclo[2.2.2]octane
280-57-9

1,4-diaza-bicyclo[2.2.2]octane

Chloroacetamide
79-07-2

Chloroacetamide

1-Carbamoylmethyl-4-aza-1-azonia-bicyclo[2.2.2]octane; chloride

1-Carbamoylmethyl-4-aza-1-azonia-bicyclo[2.2.2]octane; chloride

Conditions
ConditionsYield
In acetonitrile at 20 - 25℃;97%
With diisopropylamine In acetonitrile at 20℃; for 16h;86%

79-07-2Relevant articles and documents

Vibrational spectra of chloroacetamide and three deuterated analogues in the crystalline state

Mido, Yoshiyuki,Yanagida, Akiyo,Garcia, M. Victoria

, p. 1751 - 1758 (1993)

The IR and Raman Spectra of α-chloroacetamide CH2ClCONH2 and three deuterated analogues CH2ClCOND2, CD2ClCONH2 and CD2ClCOND2, in the crystalline state have been studied.A complete interpretation of the spectra has been worked out on the basis of spectral comparison and of the normal coordinate analysis of the four analogues.

Amide bond formation in aqueous solution: Direct coupling of metal carboxylate salts with ammonium salts at room temperature

Nielsen, John,Tung, Truong Thanh

supporting information, p. 10073 - 10080 (2021/12/10)

Herein, we report a green, expeditious, and practically simple protocol for direct coupling of carboxylate salts and ammonium salts under ACN/H2O conditions at room temperature without the addition of tertiary amine bases. The water-soluble coupling reagent EDC·HCl is a key component in the reaction. The reaction runs smoothly with unsubstituted/substituted ammonium salts and provides a clean product without column chromatography. Our reaction tolerates both carboxylate (which are unstable in other forms) and amine salts (which are unstable/volatile when present in free form). We believe that the reported method could be used as an alternative and suitable method at the laboratory and industrial scales. This journal is

A Heterogeneous Ruthenium dmso Complex Supported onto Silica Particles as a Recyclable Catalyst for the Efficient Hydration of Nitriles in Aqueous Medium

Manrique, Ester,Ferrer, Ingrid,Lu, Changyong,Fontrodona, Xavier,Rodríguez, Montserrat,Romero, Isabel

, p. 8460 - 8470 (2019/07/03)

In the present work, we describe an efficient method for the covalent anchoring of a Ru-dmso complex onto two types of supports: mesoporous silica particles (SP) and silica coated magnetic particles (MSNP). First, we have prepared and characterized the molecular complexes containing the bidentate pyridylpyrazole ligands pypz-Me and pypz-CH2COOEt, with the formula [RuIICl2(pypz-R)(dmso)2] (R = Me, 1; CH2COOEt, 2). Complex 2 was anchored onto the silica supports, yielding the heterogeneous systems SP@2 and MSNP@2 which were fully characterized by IR, UV-vis, SEM, TEM, TGA, and XPS techniques. Hydration of representative nitriles has been tested with the molecular complexes and their SP@2 and MSNP@2 heterogeneous counterparts, in aqueous medium under neutral conditions. The heterogeneous catalysts display high yields and excellent selectivity values. Both systems can be reused throughout several cycles for benzonitrile and acrylonitrile substrates, without any significant loss in reactivity. The MSNP@2 material can be easily recovered by a magnet, facilitating its reusability.

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