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Isopropylamine
Cas No: 75-31-0
USD $ 3.0-3.0 / Kilogram 1 Kilogram 1-100 Metric Ton/Month Dayang Chem (Hangzhou) Co.,Ltd. Contact Supplier
High quality Monoisopropylamine supplier in China
Cas No: 75-31-0
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IsopropylaMine;2-PropylaMine;2-AMinopropane;MonoisopropylaMine
Cas No: 75-31-0
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Isopropylamine, Monoisopropyl amine, CAS:75-31-0
Cas No: 75-31-0
No Data 1 Metric Ton Metric Ton/Month Nanjing Yuance Industry&Trade Co., Ltd. Contact Supplier
Amadis Chemical offer CAS#75-31-0;CAT#A838376
Cas No: 75-31-0
No Data 10 Milligram Amadis Chemical Co., Ltd. Contact Supplier
Isopropylamine
Cas No: 75-31-0
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Isopropylamine CAS:75-31-0
Cas No: 75-31-0
USD $ 1.0-2.0 / Metric Ton 5 Metric Ton 2500 Metric Ton/Year Henan Sinotech Import&Export Corporation Contact Supplier
Isopropylamine_
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No Data 1 Kilogram 10 Metric Ton/Month Henan Tianfu Chemical Co., Ltd. Contact Supplier
Factory Supply Isopropylamine cas 75-31-0
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No Data 200 Gram 400 Metric Ton/Day Ality Chemical Corporation Contact Supplier
Isopropylamine
Cas No: 75-31-0
No Data 1 Kilogram 300 Metric Ton/Year Jinan Finer Chemical Co., Ltd Contact Supplier

75-31-0 Usage

Reactivity Profile

Isopropylamine is a colorless, alkaline liquid, very volatile, moderately toxic, highly flammable. Dangerous fire hazard when exposed to heat, flame, sparks, or strong oxidizers. When heated to decomposition Isopropylamine emits toxic fumes of oxides of nitrogen [M. K.]. A mixture of Isopropylamine and perchloryl fluoride resulted in an uncontrolled oxidation and/or explosion, [J. Org. Chem., 1980, 45, 4036]. The reaction of 1-chloro-2,3-epoxypropane and the amine and most probably other nitrogen bases, yields a violent exotherm, [Chem. & Ind., 1971, 994].

Air & Water Reactions

Highly flammable. Water soluble.

General Description

A clear colorless liquid with an ammonia-like odor. Flash point -35°F. Boiling point 90°F. Less dense than water Vapors heavier than air. Produces toxic oxides of nitrogen during combustion. Used as a solvent and to make other chemicals.

Chemical Properties

colourless liquid

Health Hazard

Inhalation causes nose and throat irritation, severe coughing, and chest pain due to irritation of air passages; can cause lung edema and loss of consciousness. Ingestion causes nausea, salivation and severe irritation of mouth and stomach. Contact with eyes causes severe irritation and possible edema of the cornea. Contact with skin causes severe irritation.

Definition

ChEBI: A member of the class of alkylamines that is propane carrying an amino group at position 2.
InChI:InChI=1/C3H9N/c1-3(2)4/h3H,4H2,1-2H3

75-31-0 Well-known Company Product Price

Brand (Code)Product description CAS number Packaging Price Detail
Alfa Aesar (A15044)  Isopropylamine, 99+%    75-31-0 2500ml 673.0CNY Detail
Alfa Aesar (A15044)  Isopropylamine, 99+%    75-31-0 500ml 188.0CNY Detail
Alfa Aesar (A15044)  Isopropylamine, 99+%    75-31-0 100ml 159.0CNY Detail
TCI America (I0165)  Isopropylamine  >99.0%(GC)(T) 75-31-0 500mL 205.00CNY Detail
TCI America (I0165)  Isopropylamine  >99.0%(GC)(T) 75-31-0 25mL 110.00CNY Detail

75-31-0SDS

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 isopropylamine

1.2 Other means of identification

Product number -
Other names 1-Methylethylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:75-31-0 SDS

75-31-0Synthetic route

2-nitropropane
79-46-9

2-nitropropane

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With hydrogen In methanol; water at 140℃; under 30003 Torr; for 24h; Sealed tube; Autoclave;97%
With [Zn(BH4)2(py)] In tetrahydrofuran for 0.8h; Heating;94%
With poly(p-aminostyrene)-palladium(II); hydrogen In N,N-dimethyl-formamide at 70℃; under 760 Torr; for 6h;91%
methanol
67-56-1

methanol

Cp*Mo(CO)2(κ2-N,Si-iPrHNSiPh2)

Cp*Mo(CO)2(κ2-N,Si-iPrHNSiPh2)

A

Cp*(CO)2Mo(μ-OMe)(μ-H)Mo(CO)2Cp*

Cp*(CO)2Mo(μ-OMe)(μ-H)Mo(CO)2Cp*

B

dimethoxy(diphenyl)silane
6843-66-9

dimethoxy(diphenyl)silane

C

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
In benzene-d6 at 20℃; for 24h; Cooling with liquid nitrogen; Sealed tube; Inert atmosphere;A n/a
B 97%
C 74%
acetone
67-64-1

acetone

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With ammonia; hydrogen at 153℃; under 760.051 Torr; Reagent/catalyst;90.69%
With ammonia; nickel at 100℃; under 36775.4 - 55163.1 Torr; Hydrogenation;
With platinum on silica; ammonia at 240℃; Hydrogenation;
2-nitropropane
79-46-9

2-nitropropane

A

isopropylamine
75-31-0

isopropylamine

B

N-isopropylhydroxyamine
5080-22-8

N-isopropylhydroxyamine

Conditions
ConditionsYield
With hydrogen In para-xylene; isopropyl alcohol at 25℃; under 760.051 Torr; for 4h;A 9%
B 88%
1,3-diisopropylurea
4128-37-4

1,3-diisopropylurea

sodium p-toluenesulfonamide
18522-92-4

sodium p-toluenesulfonamide

A

N-(isopropylcarbamoyl)-4-methylbenzenesulfonamide
5673-38-1

N-(isopropylcarbamoyl)-4-methylbenzenesulfonamide

B

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
at 170℃; for 5h; Product distribution; other time;;A 78.2%
B n/a
at 170℃; for 5h;A 78.2%
B n/a
acetone oxime
127-06-0

acetone oxime

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With ammonium formate; zinc In methanol for 0.05h; Heating;70%
With nickel Hydrogenation.unter verschiedenen Bedingungen;
With aluminium amalgam
bis(isopropylamino)phenylborane
10475-45-3

bis(isopropylamino)phenylborane

A

(C6H5)BN(C3H7)

(C6H5)BN(C3H7)

B

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
A n/a
B 65%
A n/a
B 65%
isopropyl alcohol
67-63-0

isopropyl alcohol

A

isopropylamine
75-31-0

isopropylamine

B

diisopropylamine
108-18-9

diisopropylamine

C

acetone
67-64-1

acetone

Conditions
ConditionsYield
With ammonia; hydrogen at 160℃; under 760.051 Torr; for 0.5h; Catalytic behavior; Reagent/catalyst; Flow reactor; Inert atmosphere;A 59.9%
B n/a
C n/a
With nitrogen; ammonia; hydrogen at 170℃; Concentration; Time; Reagent/catalyst;
Bis-(trifluormethyl)-bis-(trifluormethoxy)-sulfuran
63465-11-2

Bis-(trifluormethyl)-bis-(trifluormethoxy)-sulfuran

ethylamine
75-04-7

ethylamine

A

Carbonyl fluoride
353-50-4

Carbonyl fluoride

B

hydrogen fluoride ethylamine
65756-36-7

hydrogen fluoride ethylamine

C

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
-78°C, 0.5 h;A n/a
B n/a
C 56%
methanol
67-56-1

methanol

Cp*Mo(CO)2(κ2-N,Si-iPrHNSiPh2)

Cp*Mo(CO)2(κ2-N,Si-iPrHNSiPh2)

A

methoxydiphenyl(isopropyl-amino)silane

methoxydiphenyl(isopropyl-amino)silane

B

Cp*(CO)2Mo(μ-OMe)(μ-H)Mo(CO)2Cp*

Cp*(CO)2Mo(μ-OMe)(μ-H)Mo(CO)2Cp*

C

dimethoxy(diphenyl)silane
6843-66-9

dimethoxy(diphenyl)silane

D

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
In benzene-d6 at 20℃; for 4h; Cooling with liquid nitrogen; Sealed tube; Inert atmosphere;A 11%
B 34%
C 36%
D 48%
1,4-diisopropyl-1,4-diazabuta-1,3-diene
28227-41-0, 24764-90-7

1,4-diisopropyl-1,4-diazabuta-1,3-diene

1,2-phenylenediacetonitrile
613-73-0

1,2-phenylenediacetonitrile

A

naphthalene-1,4-dicarbonitrile
3029-30-9

naphthalene-1,4-dicarbonitrile

B

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 136℃; for 1h;A 43%
B n/a
L-alanin
56-41-7

L-alanin

A

(S)-Alaninol
2749-11-3

(S)-Alaninol

B

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With phosphoric acid; hydrogen In water at 79.84℃; under 7500.75 - 60006 Torr; for 4h; Concentration; Reagent/catalyst;A 42.2%
B n/a
With sulfuric acid; hydrogen In water at 79.84℃; under 60006 Torr; for 2h; Catalytic behavior; Autoclave;
diisopropylamine
108-18-9

diisopropylamine

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
Stage #1: diisopropylamine With rhodium(III) tetra(p-sulfonato-phenyl)porphyrin; oxygen; benzaldehyde In methanol; water at 100℃; under 750.075 Torr; for 6h;
Stage #2: With hydrogenchloride In methanol; water at 80℃; Catalytic behavior;
31.2%
ramifenazone
3615-24-5

ramifenazone

A

N-Phenyl-N-(2-methylaminopropionyl)carbamic acid
13359-68-7

N-Phenyl-N-(2-methylaminopropionyl)carbamic acid

B

Methyltartronic acid anilide methylamide
16945-58-7

Methyltartronic acid anilide methylamide

C

isopropylamine
75-31-0

isopropylamine

D

Methyltartronic acid anilide isopropylamide

Methyltartronic acid anilide isopropylamide

Conditions
ConditionsYield
In water for 1728h; Irradiation;A 30%
B 22.5%
C n/a
D 8%
Benzyl-isopropyl-amin
102-97-6

Benzyl-isopropyl-amin

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
Stage #1: Benzyl-isopropyl-amin With rhodium(III) tetra(p-sulfonato-phenyl)porphyrin; oxygen; benzaldehyde In methanol; water at 100℃; under 750.075 Torr; for 6h;
Stage #2: With hydrogenchloride In methanol; water at 80℃; Catalytic behavior;
18.1%
2-iodo-propane
75-30-9

2-iodo-propane

potassium phtalimide
1074-82-4

potassium phtalimide

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
at 180 - 190℃; und Kochen des Reaktionsprodukts mit konz. HCl;
2-iodo-propane
75-30-9

2-iodo-propane

potassium cyanide
151-50-8

potassium cyanide

A

isopropylamine
75-31-0

isopropylamine

B

diisopropylamine
108-18-9

diisopropylamine

Conditions
ConditionsYield
Behandeln des Reaktionsproduktes mit Salzsaeure;
N-isopropylphthalimide
304-17-6

N-isopropylphthalimide

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With ethanol; hydrazine hydrate
acetone oxime
127-06-0

acetone oxime

A

isopropylamine
75-31-0

isopropylamine

B

diisopropylamine
108-18-9

diisopropylamine

Conditions
ConditionsYield
With hydrogen; nickel at 180 - 200℃;
propene
187737-37-7

propene

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With ammonia; sodium at 270℃; under 735508 Torr;
With ammonia; sodium at 250℃; under 661957 Torr;
With ammonia
With ammonia at 250℃; under 661957 Torr;
propene
187737-37-7

propene

A

isopropylamine
75-31-0

isopropylamine

B

diisopropylamine
108-18-9

diisopropylamine

Conditions
ConditionsYield
With ammonia at 250℃; under 661957 Torr;
diisopropyl sulfate
2973-10-6

diisopropyl sulfate

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With monoisopropyl sulfate; ammonia at 200 - 250℃; under 51485.6 - 88260.9 Torr;
diisopropyl sulfate
2973-10-6

diisopropyl sulfate

A

isopropylamine
75-31-0

isopropylamine

B

diisopropylamine
108-18-9

diisopropylamine

Conditions
ConditionsYield
With monoisopropyl sulfate; ammonia at 200 - 250℃; under 120 - 51485.6 Torr;
ISOPROPYLAMIDE
563-83-7

ISOPROPYLAMIDE

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With potassium hydroxide; bromine
1-hydroxy-2-propanone oxime
134252-16-7

1-hydroxy-2-propanone oxime

A

2-Amino-1-propanol
6168-72-5

2-Amino-1-propanol

B

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With sodium amalgam; acetic acid
1,3-dihydroxyacetone oxime
37110-18-2

1,3-dihydroxyacetone oxime

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With sodium amalgam; acetic acid
2,3-dimethyl-2,3-dinitrobutane
3964-18-9

2,3-dimethyl-2,3-dinitrobutane

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With lithium aluminium tetrahydride; diethyl ether
i-propyl isocyanide
598-45-8

i-propyl isocyanide

isopropylamine
75-31-0

isopropylamine

Conditions
ConditionsYield
With hydrogenchloride
acetic anhydride
108-24-7

acetic anhydride

isopropylamine
75-31-0

isopropylamine

N-isopropylacetamide
1118-69-0

N-isopropylacetamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; Cooling with ice;100%
With potassium carbonate; triethylamine In dichloromethane at 0 - 20℃; for 12h;89.5%
With triethylamine In dichloromethane at 20℃; for 2h;73%
benzaldehyde
100-52-7

benzaldehyde

isopropylamine
75-31-0

isopropylamine

N-benzylideneisopropylamine
6852-56-8

N-benzylideneisopropylamine

Conditions
ConditionsYield
at 20 - 100℃; for 0.133333h; microwave irradiation;100%
at 20℃; for 2h;100%
With magnesium sulfate In 1,2-dichloro-ethane at 60℃; for 18h; Glovebox;85%
benzoyl chloride
98-88-4

benzoyl chloride

isopropylamine
75-31-0

isopropylamine

N-isopropylbenzamide
5440-69-7

N-isopropylbenzamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 14h; Inert atmosphere;100%
With triethylamine In dichloromethane at 0 - 20℃; for 6h; Inert atmosphere; Schlenk technique;98%
With triethylamine In dichloromethane at 0 - 20℃; for 6h; Inert atmosphere; Schlenk technique;98%
isopropylamine
75-31-0

isopropylamine

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

N-isopropyl-p-toluenesulfonamide
21230-07-9

N-isopropyl-p-toluenesulfonamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;100%
With pyridine; dmap In dichloromethane at 0 - 20℃; for 16h;99%
With pyridine at 0 - 25℃; Inert atmosphere; Schlenk technique;99%
isopropylamine
75-31-0

isopropylamine

trifluoroacetic anhydride
407-25-0

trifluoroacetic anhydride

2,2,2-trifluoro-N-(1-methylethyl)acetamide
348-76-5

2,2,2-trifluoro-N-(1-methylethyl)acetamide

Conditions
ConditionsYield
With pyridine; dmap In tetrahydrofuran at 20℃; for 15h;100%
With diethyl ether
In diethyl ether
at 0℃; than Rt, 3 h;
In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; Glovebox;
isopropylamine
75-31-0

isopropylamine

ethyl acrylate
140-88-5

ethyl acrylate

3-isopropylaminopropionic acid ethyl ester
16217-22-4

3-isopropylaminopropionic acid ethyl ester

Conditions
ConditionsYield
In tetrahydrofuran; ethanol at 0 - 20℃; for 16h;100%
In ethanol at 0 - 20℃; for 24h;100%
With poly(ethylene glycol) 2000; ruthenium trichloride at 50℃; for 8h; aza-Michael addition;91%
isopropylamine
75-31-0

isopropylamine

ethyl 2-cyanoacetate
105-56-6

ethyl 2-cyanoacetate

2-cyano-N-isopropylacetamide
52573-74-7

2-cyano-N-isopropylacetamide

Conditions
ConditionsYield
for 18h;100%
With sodium hydroxide
2,4,6-Tris(4-methylphenoxy)-1,3,5-triazine
1177-35-1

2,4,6-Tris(4-methylphenoxy)-1,3,5-triazine

isopropylamine
75-31-0

isopropylamine

(4,6-Bis-p-tolyloxy-[1,3,5]triazin-2-yl)-isopropyl-amine
79922-84-2

(4,6-Bis-p-tolyloxy-[1,3,5]triazin-2-yl)-isopropyl-amine

Conditions
ConditionsYield
100%
4-methoxy-benzaldehyde
123-11-5

4-methoxy-benzaldehyde

isopropylamine
75-31-0

isopropylamine

N-(2-propyl)-4-methoxybenzylideneamine
13033-52-8

N-(2-propyl)-4-methoxybenzylideneamine

Conditions
ConditionsYield
In chloroform at 20℃; for 24h;100%
at 20 - 100℃; for 0.133333h; microwave irradiation;85%
at 20℃; for 48h;83%
N,N-dimethyl-formamide dimethyl acetal
4637-24-5

N,N-dimethyl-formamide dimethyl acetal

isopropylamine
75-31-0

isopropylamine

N2-iso-propyl-N1,N1-dimethylformamidine
32150-24-6

N2-iso-propyl-N1,N1-dimethylformamidine

Conditions
ConditionsYield
at 60℃;100%
1,1,1,3,3,3-hexachloro-propan-2-one
116-16-5

1,1,1,3,3,3-hexachloro-propan-2-one

isopropylamine
75-31-0

isopropylamine

A

chloroform
67-66-3

chloroform

B

N-Isopropyl-2,2,2-trichloroacetamide
23144-67-4

N-Isopropyl-2,2,2-trichloroacetamide

Conditions
ConditionsYield
In hexaneA n/a
B 100%
isopropylamine
75-31-0

isopropylamine

methyl β-isopropylaminobutanoate
161722-25-4

methyl β-isopropylaminobutanoate

Conditions
ConditionsYield
zirconium(IV) chloride In acetonitrile at 30℃; under 750.06 Torr; for 24h; Product distribution; var. α,β-unsat. ester, catalyst, pressure, temp.;100%
zirconium(IV) chloride In acetonitrile at 30℃; under 750.06 Torr; for 24h;100%
In acetone for 30h; Heating;
1,3-dibromo-pentan-2-one
816-21-7

1,3-dibromo-pentan-2-one

isopropylamine
75-31-0

isopropylamine

Bis-(N-isopropyl)pentane-1,2-diimine
81981-83-1

Bis-(N-isopropyl)pentane-1,2-diimine

Conditions
ConditionsYield
In pentane for 22h;100%
With magnesium sulfate In pentane for 22h; Ambient temperature;96%
pentachloroacetone
1768-31-6

pentachloroacetone

isopropylamine
75-31-0

isopropylamine

A

chloroform
67-66-3

chloroform

B

N-Isopropyl-2,2-dichloroacetamide
39063-24-6

N-Isopropyl-2,2-dichloroacetamide

Conditions
ConditionsYield
In hexane for 0.5h;A n/a
B 100%
(E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-one
59938-06-6

(E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-one

isopropylamine
75-31-0

isopropylamine

(Z)-1,1,1-Trifluoro-4-isopropylamino-but-3-en-2-one
127223-90-9

(Z)-1,1,1-Trifluoro-4-isopropylamino-but-3-en-2-one

Conditions
ConditionsYield
In acetonitrile Ambient temperature;100%
(2-formylphenyl)(diphenyl)phosphine
50777-76-9

(2-formylphenyl)(diphenyl)phosphine

isopropylamine
75-31-0

isopropylamine

isopropylamine

isopropylamine

Conditions
ConditionsYield
In methanol; dichloromethane at 20℃; for 2h; Inert atmosphere;100%
In toluene at 150 - 160℃; for 6h; Inert atmosphere;97%
In methanol; dichloromethane at 20℃; for 3h;83%
for 4h; Heating;80%
(S)-(1-naphthyl) glycidyl ether
61249-00-1

(S)-(1-naphthyl) glycidyl ether

isopropylamine
75-31-0

isopropylamine

(S)-1-isopropylamino-3-(1-naphthyloxy)-2-propanol
4199-09-1

(S)-1-isopropylamino-3-(1-naphthyloxy)-2-propanol

Conditions
ConditionsYield
In water for 3h; Heating;100%
In water for 1h; Heating;99%
With Na-zeolite In acetonitrile at 20℃; for 12h;95%
N,N-Dimethyl-2,4-bis(trifluoroacetyl)-1-naphthylamine
115975-33-2

N,N-Dimethyl-2,4-bis(trifluoroacetyl)-1-naphthylamine

isopropylamine
75-31-0

isopropylamine

2,2,2-Trifluoro-1-[4-isopropylamino-3-(2,2,2-trifluoro-acetyl)-naphthalen-1-yl]-ethanone
115975-38-7

2,2,2-Trifluoro-1-[4-isopropylamino-3-(2,2,2-trifluoro-acetyl)-naphthalen-1-yl]-ethanone

Conditions
ConditionsYield
In acetonitrile for 2h; Ambient temperature;100%
N-ethoxycarbonylaminomethylphosphonic acid
128336-73-2

N-ethoxycarbonylaminomethylphosphonic acid

isopropylamine
75-31-0

isopropylamine

(Ethoxycarbonylamino-methyl)-phosphonic acid; compound with isopropylamine
128336-79-8

(Ethoxycarbonylamino-methyl)-phosphonic acid; compound with isopropylamine

Conditions
ConditionsYield
In ethanol100%
N-(triethylstannyl)succinimide
53583-75-8

N-(triethylstannyl)succinimide

isopropylamine
75-31-0

isopropylamine

N-isopropylsuccinamide
3026-11-7

N-isopropylsuccinamide

Conditions
ConditionsYield
In methanol at 90℃; for 2h;100%
N-Boc-cyclohexylnorstatin
105116-44-7

N-Boc-cyclohexylnorstatin

isopropylamine
75-31-0

isopropylamine

Boc-cyclohexylnorstatine isopropylamide
119600-98-5

Boc-cyclohexylnorstatine isopropylamide

Conditions
ConditionsYield
With N-hydroxy-5-norbornene-2,3-dicarboximide; dicyclohexyl-carbodiimide In ethyl acetate Ambient temperature;100%
N-Isopropyl-N-((1E,3E)-6,6,6-trifluoro-5-oxo-hexa-1,3-dienyl)-acetamide
104429-28-9

N-Isopropyl-N-((1E,3E)-6,6,6-trifluoro-5-oxo-hexa-1,3-dienyl)-acetamide

isopropylamine
75-31-0

isopropylamine

(3E,5E)-1,1,1-Trifluoro-6-isopropylamino-hexa-3,5-dien-2-one
132630-54-7

(3E,5E)-1,1,1-Trifluoro-6-isopropylamino-hexa-3,5-dien-2-one

Conditions
ConditionsYield
In acetonitrile for 4h; Ambient temperature;100%
2-m-chlorobenzoyloxy-4-isopropyl-2H-1,4-thiazin-3-one
82912-51-4

2-m-chlorobenzoyloxy-4-isopropyl-2H-1,4-thiazin-3-one

isopropylamine
75-31-0

isopropylamine

4-Isopropyl-2-isopropylamino-4H-[1,4]thiazin-3-one
85331-45-9

4-Isopropyl-2-isopropylamino-4H-[1,4]thiazin-3-one

Conditions
ConditionsYield
for 24h; Ambient temperature;100%
isopropylamine
75-31-0

isopropylamine

(S)-(+)-1-chloro-3-(1-naphthyloxy)-2-propanol
132005-35-7

(S)-(+)-1-chloro-3-(1-naphthyloxy)-2-propanol

(R)-propranolol hydrochloride
318-98-9, 3506-09-0, 4199-10-4, 13071-11-9

(R)-propranolol hydrochloride

Conditions
ConditionsYield
With sodium hydroxide; water for 16h; Ambient temperature;100%
(R)-(-)-1-chloro-2-acetoxy-3-(1-naphthyloxy)propane
108508-19-6

(R)-(-)-1-chloro-2-acetoxy-3-(1-naphthyloxy)propane

isopropylamine
75-31-0

isopropylamine

(S)-(-)-propanolol hydrochloride
4199-10-4

(S)-(-)-propanolol hydrochloride

Conditions
ConditionsYield
With sodium hydroxide; water for 16h; Ambient temperature;100%
2-Chloro-3-<α-cyano-α-(benzimidazol-2-yl)methylene>3,4-dihydroquinoxaline
125103-12-0

2-Chloro-3-<α-cyano-α-(benzimidazol-2-yl)methylene>3,4-dihydroquinoxaline

isopropylamine
75-31-0

isopropylamine

1-Isopropyl-2-Amino-3-(benzimidazol-2-yl)pyrrolo<2,3-b>quinoxaline
120340-83-2

1-Isopropyl-2-Amino-3-(benzimidazol-2-yl)pyrrolo<2,3-b>quinoxaline

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 130℃; for 4h; sealed ampul;100%
(+/-)-threo 2,3-epoxy-1-phenylphospholane 1-oxide
142386-32-1, 142435-86-7

(+/-)-threo 2,3-epoxy-1-phenylphospholane 1-oxide

isopropylamine
75-31-0

isopropylamine

(1S,2R,3R)-2-Isopropylamino-1-oxo-1-phenyl-1λ5-phospholan-3-ol
142386-34-3

(1S,2R,3R)-2-Isopropylamino-1-oxo-1-phenyl-1λ5-phospholan-3-ol

Conditions
ConditionsYield
In methanol at 40℃; Ring cleavage; addition;100%
at 40℃; for 48h;
1-(octylthio)carbonyl-3-(tetrahydrofuryl)-5-fluorouracil
90162-90-6

1-(octylthio)carbonyl-3-(tetrahydrofuryl)-5-fluorouracil

isopropylamine
75-31-0

isopropylamine

5-fluoro-3-(tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
63901-83-7

5-fluoro-3-(tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

Conditions
ConditionsYield
In diethyl ether for 0.166667h; Ambient temperature;100%
Toluene-4-sulfonic acid (S)-2-hydroxy-3-(2-methyl-3-nitro-phenoxy)-propyl ester
81102-68-3

Toluene-4-sulfonic acid (S)-2-hydroxy-3-(2-methyl-3-nitro-phenoxy)-propyl ester

isopropylamine
75-31-0

isopropylamine

<2R>-(+)-1-isopropylamino-3-(2-methyl-3-nitrophenoxy)-2-propanol
81132-32-3

<2R>-(+)-1-isopropylamino-3-(2-methyl-3-nitrophenoxy)-2-propanol

Conditions
ConditionsYield
In toluene for 10h; Heating;100%
1-ethylthio-4,4-bis(trifluoroacetyl)-1,3-butadiene
132630-60-5

1-ethylthio-4,4-bis(trifluoroacetyl)-1,3-butadiene

isopropylamine
75-31-0

isopropylamine

3-trifluoroacetyl-2-trifluoromethyl-2-hydroxy-1-isopropyl-1,2-dihydropyridine

3-trifluoroacetyl-2-trifluoromethyl-2-hydroxy-1-isopropyl-1,2-dihydropyridine

Conditions
ConditionsYield
In acetonitrile for 1h; Ambient temperature;100%

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