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108-49-6 Usage

Chemical Properties

White to pale yellow crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 108-49-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108-49:
(5*1)+(4*0)+(3*8)+(2*4)+(1*9)=46
46 % 10 = 6
So 108-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2/c1-5-3-7-4-6(2)8-5/h5-8H,3-4H2,1-2H3/t5-,6-/m0/s1

108-49-6 Well-known Company Product Price

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  • Aldrich

  • (D179809)  2,6-Dimethylpiperazine  97%

  • 108-49-6

  • D179809-1G

  • 340.47CNY

  • Detail
  • Aldrich

  • (D179809)  2,6-Dimethylpiperazine  97%

  • 108-49-6

  • D179809-5G

  • 1,304.55CNY

  • Detail
  • Aldrich

  • (D179809)  2,6-Dimethylpiperazine  97%

  • 108-49-6

  • D179809-25G

  • 4,266.99CNY

  • Detail

108-49-6SDS

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 2,6-Dimethylpiperazine

1.2 Other means of identification

Product number -
Other names 2,6-di-methylpiperazine

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:108-49-6 SDS

108-49-6Synthetic route

1,4-dinitroso-2,6-dimethylpiperazine
55380-34-2

1,4-dinitroso-2,6-dimethylpiperazine

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
With hydrogenchloride; ammonium sulphamate at 50℃; Rate constant; piperidinium perchlorate, 18h; transnitrosating studies;
N-nitroso-3,5-dimethylpiperazine
67774-31-6

N-nitroso-3,5-dimethylpiperazine

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
With hydrogenchloride; ammonium sulphamate at 50℃; Rate constant;
C6H13(2)HN2

C6H13(2)HN2

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
With water-d2 In water at 34.9℃; Equilibrium constant;
C6H13(2)HN2

C6H13(2)HN2

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
With water-d2 In water at 34.9℃; Equilibrium constant;
Acetol acetate
592-20-1

Acetol acetate

ammonia
7664-41-7

ammonia

water
7732-18-5

water

Raney nickel

Raney nickel

hydrogen

hydrogen

A

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

B

bis-acetoxypropyl-amines

bis-acetoxypropyl-amines

Conditions
ConditionsYield
at 200℃; 90 at Anfangsdruck bei 25grad;
glycerol
56-81-5

glycerol

A

piperazine
110-85-0

piperazine

B

N-(1-aminomethyl-2-hydroxyethyl)amine
2811-20-3

N-(1-aminomethyl-2-hydroxyethyl)amine

C

1,2,3-triaminopropane
21291-99-6

1,2,3-triaminopropane

D

(RS)-2-methylpiperazine
109-07-9

(RS)-2-methylpiperazine

E

ethylenediamine
107-15-3

ethylenediamine

F

1,2-diaminopropan
78-90-0, 10424-38-1

1,2-diaminopropan

G

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
With ammonia; hydrogen; Raney nickel In water at 200℃; under 15001.5 - 150015 Torr; Product distribution / selectivity; Autoclave;
glycerol
56-81-5

glycerol

A

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

2-Amino-1-propanol

B

N-(1-aminomethyl-2-hydroxyethyl)amine
2811-20-3

N-(1-aminomethyl-2-hydroxyethyl)amine

C

1,2,3-triaminopropane
21291-99-6

1,2,3-triaminopropane

D

(RS)-2-methylpiperazine
109-07-9

(RS)-2-methylpiperazine

E

1,2-diaminopropan
78-90-0, 10424-38-1

1,2-diaminopropan

F

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

G

2,5-dimethylpiperazine
106-55-8

2,5-dimethylpiperazine

Conditions
ConditionsYield
With ammonia; hydrogen; catalyst precursor whose active composition comprised 13% by weight of Cu, calculated as CuO, 28% by weight of Ni, calculated as NiO, 28% by weight of Co, calculated as CoO and 31% by weight of Zr, calculated as ZrO2 In water at 180℃; under 150015 Torr; for 53h; Product distribution / selectivity;
glycerol
56-81-5

glycerol

A

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

2-Amino-1-propanol

B

N-(1-aminomethyl-2-hydroxyethyl)amine
2811-20-3

N-(1-aminomethyl-2-hydroxyethyl)amine

C

1,2,3-triaminopropane
21291-99-6

1,2,3-triaminopropane

D

2-aminomethyl-6-methylpiperazine
1122585-40-3

2-aminomethyl-6-methylpiperazine

E

2,5-bis(aminomethyl)piperazine
1122585-41-4

2,5-bis(aminomethyl)piperazine

F

2-aminomethylpiperazine
130861-85-7

2-aminomethylpiperazine

G

2-aminomethyl-5-methylpiperazine
136665-35-5

2-aminomethyl-5-methylpiperazine

H

(RS)-2-methylpiperazine
109-07-9

(RS)-2-methylpiperazine

I

1,2-diaminopropan
78-90-0, 10424-38-1

1,2-diaminopropan

J

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

K

2,5-dimethylpiperazine
106-55-8

2,5-dimethylpiperazine

Conditions
ConditionsYield
With ammonia; hydrogen; catalyst precursor whose active composition comprised 50% by weight of Ni, calculated as NiO, 18% by weight of Cu, calculated as CuO, 2% by weight of Mo, calculated as MoO3, and 30% by weight or Zr, calculated as ZrO2 In water at 192℃; under 150015 Torr; for 1076h; Product distribution / selectivity;
D-glucose
50-99-7

D-glucose

A

piperazine
110-85-0

piperazine

B

(RS)-2-methylpiperazine
109-07-9

(RS)-2-methylpiperazine

C

ethylenediamine
107-15-3

ethylenediamine

D

1,2-diaminopropan
78-90-0, 10424-38-1

1,2-diaminopropan

E

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
Stage #1: D-glucose With hydrogen; calcium oxide In water at 230℃; under 75007.5 - 187519 Torr; for 10h; Autoclave; Inert atmosphere;
Stage #2: With ammonia; hydrogen In water at 100 - 200℃; under 15001.5 - 150015 Torr; for 36h; Product distribution / selectivity; Autoclave; Inert atmosphere;
D-sorbitol
50-70-4

D-sorbitol

A

(RS)-2-methylpiperazine
109-07-9

(RS)-2-methylpiperazine

B

ethylenediamine
107-15-3

ethylenediamine

C

1,2-diaminopropan
78-90-0, 10424-38-1

1,2-diaminopropan

D

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
With ammonia; hydrogen; reduced catalyst comprising 13 wtpercent Cu (calculated as CuO), 28 wtpercent Ni (calculated as NiO), 28 wtpercent Co (calculated as CoO), 31 wtpercent Zr (calculated as ZrO2) In water at 100 - 190℃; under 15001.5 - 150015 Torr; for 36h; Product distribution / selectivity; Autoclave; Inert atmosphere;
D-sorbitol
50-70-4

D-sorbitol

A

piperazine
110-85-0

piperazine

B

(RS)-2-methylpiperazine
109-07-9

(RS)-2-methylpiperazine

C

ethylenediamine
107-15-3

ethylenediamine

D

1,2-diaminopropan
78-90-0, 10424-38-1

1,2-diaminopropan

E

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

F

2,5-dimethylpiperazine
106-55-8

2,5-dimethylpiperazine

Conditions
ConditionsYield
With ammonia; hydrogen; reduced catalyst comprising 13 wtpercent Cu (calculated as CuO), 28 wtpercent Ni (calculated as NiO), 28 wtpercent Co (calculated as CoO), 31 wtpercent Zr (calculated as ZrO2) In water at 100 - 200℃; under 15001.5 - 150015 Torr; for 36h; Product distribution / selectivity; Autoclave; Inert atmosphere;
propylene glycol
57-55-6

propylene glycol

A

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

2-Amino-1-propanol

B

3-amino-2-propanol
78-96-6, 1674-56-2

3-amino-2-propanol

C

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

D

2,5-dimethylpiperazine
106-55-8

2,5-dimethylpiperazine

Conditions
ConditionsYield
With ammonium hydroxide; hydrogen In water at 179.84℃; under 7500.75 Torr; for 24h; Catalytic behavior; Reagent/catalyst; Autoclave; Inert atmosphere;
1,2-diaminopropan
78-90-0, 10424-38-1

1,2-diaminopropan

glycerol
56-81-5

glycerol

A

2,6-dimethylpyrazine
108-50-9

2,6-dimethylpyrazine

B

2-hydroxymethyl-6-methylpyrazine
77164-93-3

2-hydroxymethyl-6-methylpyrazine

C

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
With CuCrimp In water at 375℃; under 760.051 Torr; Kinetics; Catalytic behavior; Reagent/catalyst; Flow reactor;
With Nano-crystalline mixed oxides of ZnO-ZnCr2O4 In water at 375℃; under 760.051 Torr; Kinetics; Reagent/catalyst; Flow reactor; Inert atmosphere;
propylene glycol
57-55-6

propylene glycol

A

2,5-dimethyl-pyrazine
123-32-0

2,5-dimethyl-pyrazine

B

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

2-Amino-1-propanol

C

(R)-(-)-2-amino-2-propanol
14008-30-1

(R)-(-)-2-amino-2-propanol

D

1,2-diaminopropan
78-90-0, 10424-38-1

1,2-diaminopropan

E

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Conditions
ConditionsYield
With ammonia; hydrogen at 170 - 375℃; under 60006 Torr; for 50h;
With ammonia; hydrogen at 230 - 375℃; under 60006 Torr; for 50h;
With ammonia; hydrogen at 160 - 375℃; under 30003 Torr; for 50h;
With ammonia; hydrogen at 160 - 375℃; under 45004.5 Torr; for 50h;
With ammonia; hydrogen at 160 - 375℃; under 60006 Torr; for 50h;
1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
93107-30-3

1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

PD158804
93107-34-7

PD158804

Conditions
ConditionsYield
In pyridine Heating;100%
3-bromo-N,N-bis(4-fluorophenyl)propanamide
95017-63-3

3-bromo-N,N-bis(4-fluorophenyl)propanamide

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

3-(3,5-dimethyl-piperazin-1-yl)-N,N-bis-(4-fluoro-phenyl)-propionamide

3-(3,5-dimethyl-piperazin-1-yl)-N,N-bis-(4-fluoro-phenyl)-propionamide

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 2h;100%
di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

1-(1,1-Dimethylethoxycarbonyl)-cis-3,5-dimethylpiperazine
639068-43-2

1-(1,1-Dimethylethoxycarbonyl)-cis-3,5-dimethylpiperazine

Conditions
ConditionsYield
dmap In dichloromethane100%
With triethylamine In dichloromethane at 0 - 20℃; for 12h;56%
In ethanol; water
benzoyl chloride
98-88-4

benzoyl chloride

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

(2,6-dimethylpiperazin-1-yl)(phenyl)methanone
4143-57-1

(2,6-dimethylpiperazin-1-yl)(phenyl)methanone

Conditions
ConditionsYield
With n-butyllithium; chloro-trimethyl-silane In tetrahydrofuran99%
benzoyl chloride
98-88-4

benzoyl chloride

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

N-(benzoyl)-cis-2,6-dimethylpiperazine

N-(benzoyl)-cis-2,6-dimethylpiperazine

Conditions
ConditionsYield
Stage #1: 3,5-dimethylpiperazine With n-butyllithium In tetrahydrofuran at 20℃; for 0.5h; Metallation;
Stage #2: With triethylsilyl chloride In tetrahydrofuran at 20℃; for 1h; silylation;
Stage #3: benzoyl chloride In tetrahydrofuran at 20℃; for 0.166667h; benzoylation; Further stages.;
99%
2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

4-chloro-7-azaindole
55052-28-3

4-chloro-7-azaindole

4-(3,5-dimethylpiperazin-1-yl)-1H-pyrrolo[2,3-b]pyridine
1248587-59-8

4-(3,5-dimethylpiperazin-1-yl)-1H-pyrrolo[2,3-b]pyridine

Conditions
ConditionsYield
With RuPhos palladacycle; lithium hexamethyldisilazane; ruphos In tetrahydrofuran at 65℃; for 4h; Inert atmosphere; Sealed vial;99%
1,3-diacetyl-1,3-dihydro-benzoimidazol-2-one
2735-73-1

1,3-diacetyl-1,3-dihydro-benzoimidazol-2-one

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

1-(3,5-Dimethyl-piperazin-1-yl)-ethanone

1-(3,5-Dimethyl-piperazin-1-yl)-ethanone

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 0.3h;98%
1-bromo-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethane-1-sulfonyl fluoride

1-bromo-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethane-1-sulfonyl fluoride

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

(E)-2-(3,5-dimethylpiperazin-1-yl)ethene-1-sulfonyl fluoride

(E)-2-(3,5-dimethylpiperazin-1-yl)ethene-1-sulfonyl fluoride

Conditions
ConditionsYield
In 1,4-dioxane at 20℃; stereoselective reaction;96%
1-(2-methoxyphenyl)-3,5-bis(trichloromethyl)triazine

1-(2-methoxyphenyl)-3,5-bis(trichloromethyl)triazine

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

2-(3,5-dimethylpiperazin-1-yl)-4-(2-methoxyphenyl)-6-trichloromethyl[1,3,5]triazine

2-(3,5-dimethylpiperazin-1-yl)-4-(2-methoxyphenyl)-6-trichloromethyl[1,3,5]triazine

Conditions
ConditionsYield
With sodium hydrogencarbonate In DMF (N,N-dimethyl-formamide) at 20℃;95%
2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

6,7-difluoro-1-(2-fluoro-4-nitrophenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
353794-08-8

6,7-difluoro-1-(2-fluoro-4-nitrophenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

7-(dimethyl-piperazin-1-yl)-6-fluoro-1-(2-fluoro-4-nitro-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

7-(dimethyl-piperazin-1-yl)-6-fluoro-1-(2-fluoro-4-nitro-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

Conditions
ConditionsYield
With triethylamine In acetonitrile Heating;93%
6,7-Difluoro-4-oxo-1-o-tolyl-1,4-dihydro-quinoline-3-carboxylic acid
1026984-41-7

6,7-Difluoro-4-oxo-1-o-tolyl-1,4-dihydro-quinoline-3-carboxylic acid

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

7-(3,5-Dimethyl-piperazin-1-yl)-6-fluoro-4-oxo-1-o-tolyl-1,4-dihydro-quinoline-3-carboxylic acid

7-(3,5-Dimethyl-piperazin-1-yl)-6-fluoro-4-oxo-1-o-tolyl-1,4-dihydro-quinoline-3-carboxylic acid

Conditions
ConditionsYield
In acetonitrile92%
4-nitro-benzoyl chloride
122-04-3

4-nitro-benzoyl chloride

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

N1-(4-nitrobenzoyl)-2,6-dimethylpiperazine

N1-(4-nitrobenzoyl)-2,6-dimethylpiperazine

Conditions
ConditionsYield
Stage #1: 3,5-dimethylpiperazine With n-butyllithium In tetrahydrofuran at 20℃; for 0.5h; Inert atmosphere;
Stage #2: With chloro-trimethyl-silane In tetrahydrofuran at 20℃; for 1h;
Stage #3: 4-nitro-benzoyl chloride In tetrahydrofuran at 20℃; for 0.166667h;
90%
Stage #1: 3,5-dimethylpiperazine With n-butyllithium In tetrahydrofuran at 20℃; for 0.5h; Inert atmosphere;
Stage #2: With chloro-trimethyl-silane In tetrahydrofuran for 1h;
Stage #3: 4-nitro-benzoyl chloride In tetrahydrofuran for 0.166667h;
90%
1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
75338-42-0

1-ethyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

7-(3,5-Dimethyl-piperazin-1-yl)-1-ethyl-6,8-difluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
98079-68-6

7-(3,5-Dimethyl-piperazin-1-yl)-1-ethyl-6,8-difluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

Conditions
ConditionsYield
With triethylamine In acetonitrile Heating;89%
Cholesteryl chloroformate
7144-08-3

Cholesteryl chloroformate

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

cholest-5-en-3-yl 3,5-dimethyl-1-piperazinecarboxylate
1120327-12-9

cholest-5-en-3-yl 3,5-dimethyl-1-piperazinecarboxylate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;89%
In dichloromethane at 0 - 20℃;
2,6-dichloro-4-cyclopropylpyridine-3,5-dicarbonitrile

2,6-dichloro-4-cyclopropylpyridine-3,5-dicarbonitrile

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

2-chloro-4-cyclopropyl-6-(3,5-dimethylpiperazin-1-yl)pyridine-3,5-dicarbonitrile

2-chloro-4-cyclopropyl-6-(3,5-dimethylpiperazin-1-yl)pyridine-3,5-dicarbonitrile

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 20℃; for 0.0833333h;89%
2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

5-bromo-2-chloro-4-methylpyridine
778611-64-6

5-bromo-2-chloro-4-methylpyridine

1-(5-bromo-4-methylpyridin-2-yl)-3,5-dimethylpiperazine

1-(5-bromo-4-methylpyridin-2-yl)-3,5-dimethylpiperazine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dimethyl sulfoxide at 100℃; for 16h;87.3%
6,7-difluoro-1-(2,4-difluorophenyl)-1,4-dihydro-4-oxo-3-quinoline-carboxylic acid
103995-01-3

6,7-difluoro-1-(2,4-difluorophenyl)-1,4-dihydro-4-oxo-3-quinoline-carboxylic acid

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

PD 160338

PD 160338

Conditions
ConditionsYield
In acetonitrile86%
1-ethyl-6,7-difluoro-8-chloro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
80076-53-5

1-ethyl-6,7-difluoro-8-chloro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

8-Chloro-7-(3,5-dimethyl-piperazin-1-yl)-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
131683-65-3

8-Chloro-7-(3,5-dimethyl-piperazin-1-yl)-1-ethyl-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 60℃;85%
1-ethyl-6,7,8-trifluoro-1,4-dihydro-5-hydroxy-4-oxo-3-quinolinecarboxylic acid
131684-01-0

1-ethyl-6,7,8-trifluoro-1,4-dihydro-5-hydroxy-4-oxo-3-quinolinecarboxylic acid

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

7-(3,5-Dimethyl-piperazin-1-yl)-1-ethyl-6,8-difluoro-5-hydroxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
131683-88-0

7-(3,5-Dimethyl-piperazin-1-yl)-1-ethyl-6,8-difluoro-5-hydroxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

Conditions
ConditionsYield
With triethylamine In acetonitrile Heating;85%
6,7-difluoro-4-oxo-1-(propan-2-yl)-1,4-dihydroquinoline-3-carboxylic acid
174358-43-1

6,7-difluoro-4-oxo-1-(propan-2-yl)-1,4-dihydroquinoline-3-carboxylic acid

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

PD 163755

PD 163755

Conditions
ConditionsYield
In acetonitrile for 17h; Heating;85%
uranyl thiocyanate hexahydrate

uranyl thiocyanate hexahydrate

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

UO2(2+)*2NCS(1-)*0.5(CH3)2C4H8N2*C2H5OH=UO2(NCS)2((CH3)2C4H8N2)0.5(C2H5OH)

UO2(2+)*2NCS(1-)*0.5(CH3)2C4H8N2*C2H5OH=UO2(NCS)2((CH3)2C4H8N2)0.5(C2H5OH)

Conditions
ConditionsYield
With ethanol In ethanol a soln. of the ligand in abs. ethanol was added dropwise with constant shaking to an ethanolic soln. of UO2-salt; excess of ether was added to complete pptn., ppt. was filtered under anhyd. conditions, washed with ethanol and ether, dried under vac.; elem. anal.;85%
neodymium(III) nitrate
16454-60-7

neodymium(III) nitrate

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

(Nd(NO3)3(C4H8N2(CH3)2)0.5(CH3OH)2)2

(Nd(NO3)3(C4H8N2(CH3)2)0.5(CH3OH)2)2

Conditions
ConditionsYield
With CH3OH In methanol soln. of Nd(NO3)3 in methanol/2,2'-dimethoxypropane was refluxed, cooling to room temp., addn. of a soln. of ligand in methanol with shaking;; ppt. was sepd., washed, filtered and dried; elem. anal.;;85%
6-bromo-N-(6-methoxy-4-methyl-8-quinolinyl)-hexanamide
75464-75-4

6-bromo-N-(6-methoxy-4-methyl-8-quinolinyl)-hexanamide

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

N-(6-Methoxy-4-methyl-8-quinolinyl)-3,5-dimethyl-1-piperazine-hexanamide
83547-07-3

N-(6-Methoxy-4-methyl-8-quinolinyl)-3,5-dimethyl-1-piperazine-hexanamide

Conditions
ConditionsYield
In benzene for 25h; Heating;83%
With sodium hydroxide; triethylamine In benzene5 g (83%)
1-(methylsufonyl)-4-fluorobenzene
455-15-2

1-(methylsufonyl)-4-fluorobenzene

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

(3R,5S)-3,5-dimethyl-1-[4-(methylsulfonyl)phenyl]piperazine
1095538-53-6

(3R,5S)-3,5-dimethyl-1-[4-(methylsulfonyl)phenyl]piperazine

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 100℃; for 4h;83%
Pentafluoropyridine
700-16-3

Pentafluoropyridine

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

3,5-dimethyl-1-(perfluoropyridin-4-yl)piperazine

3,5-dimethyl-1-(perfluoropyridin-4-yl)piperazine

Conditions
ConditionsYield
In ethanol at 0℃; for 168h;82%
1-(2,4-Dichloro-phenyl)-6,7-difluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
1026747-59-0

1-(2,4-Dichloro-phenyl)-6,7-difluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

1-(2,4-Dichloro-phenyl)-7-(dimethyl-piperazin-1-yl)-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

1-(2,4-Dichloro-phenyl)-7-(dimethyl-piperazin-1-yl)-6-fluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid

Conditions
ConditionsYield
In acetonitrile81%
o-bromobenzenesulfonyl chloride
2905-25-1

o-bromobenzenesulfonyl chloride

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

racemic-1-((2-bromophenyl)sulfonyl)-3,5-dimethylpiperazine

racemic-1-((2-bromophenyl)sulfonyl)-3,5-dimethylpiperazine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.25h; Inert atmosphere;81%
2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

3-[1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinoline-2-carbonyl]-1-methyl-3H-imidazol-1-ium; iodide

3-[1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinoline-2-carbonyl]-1-methyl-3H-imidazol-1-ium; iodide

N,N'-bis-[2-carbamoyl-1-(3,4-dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolinyl]-2,6-dimethylpiperazine

N,N'-bis-[2-carbamoyl-1-(3,4-dimethoxybenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolinyl]-2,6-dimethylpiperazine

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃;80%
neodymium trichloride
10024-93-8

neodymium trichloride

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

Nd(3+)*3Cl(1-)*C4H8N2(CH3)2*C2H5OH=NdCl3(C4H8N2(CH3)2)(C2H5OH)

Nd(3+)*3Cl(1-)*C4H8N2(CH3)2*C2H5OH=NdCl3(C4H8N2(CH3)2)(C2H5OH)

Conditions
ConditionsYield
With ethanol In ethanol shaking of the ligand and metal salt (2:1 molar ratio) in abs. ethanol;; ppt. was washed with ethanol and Et2O, filtered, dried under vac.; elem. anal.;;80%
copper(II) ortho-methylbenzoate
5819-24-9, 64508-54-9

copper(II) ortho-methylbenzoate

2,6-dimethylpiperazine
108-49-6

2,6-dimethylpiperazine

[di(ortho-toluato)(2,6-dimethylpiperazine)copper(II)]n

[di(ortho-toluato)(2,6-dimethylpiperazine)copper(II)]n

Conditions
ConditionsYield
In diethyl ether to suspn. of copper salt soln. of base (stoich. amt.) added dropwise after successive intervals of 10 min over a total period of ca. 2.5 h understirring, mixt. stirred for another 2 h; mixt. cooled, ppt. filtered, washed with acetone and diethyl ether, dried in vac.; elem. anal.;80%

108-49-6Relevant articles and documents

CuCr2O4 derived by the sol-gel method as a highly active and selective catalyst for the conversion of glycerol to 2,6-dimethylpyrazine: A benign and eco-friendly process

Vankudoth, Krishna,Gutta, Naresh,Velisoju, Vijay Kumar,Mutyala, Suresh,Aytam, Hari Padmasri,Akula, Venugopal

, p. 3399 - 3407 (2017)

Vapour phase dehydrocyclization of crude glycerol in conjunction with 1,2-propanediamine (1,2-PDA) was examined over CuCr2O4 obtained by different preparation methods. A high proportion of copper species interacted with Cr2O3 in CuCr2O4 derived from the sol-gel route with a low ratio of Cu2+/Cu0 demonstrating higher dehydrocyclization activity and 2,6-dimethylpyrazine (2,6-DMP) selectivity. X-ray photoelectron spectroscopy analysis of the reduced CuCr2O4 revealed a lower fraction of ionic Cu and a high percentage of metallic Cu in the near surface region. The HCOOH and pyridine adsorbed DRIFT spectra of CuCr2O4 revealed that strong basic and moderate Lewis acid sites are responsible for the selective formation of 2,6-dimethylpyrazine which is consistent with the catalyst poisoning studies on CuCr2O4 co-feeding with pyridine as both Br?nsted and Lewis acid site blocker and 2,6-lutidine as a selective Br?nsted acid site blocker during the dehydrocyclization reaction. The presence of isolated CuO and Cr2O3 species led to a high selectivity for 2,6-dimethylpiperazine. The high intrinsic activity of CuCrsol-gel was also concomitant with the Cu metal surface areas of the catalysts. The fresh, reduced and some of the used catalysts are characterized by BET-surface area, powder XRD, FTIR, XPS, TEM, H2-TPR, TPD of NH3, pyridine, 2,6-dimethylpyridine and HCOOH adsorbed DRIFT spectroscopy.

The invention relates to a propylene glycol and liquid ammonia as raw materials for preparing propylene diamine method and apparatus thereof

-

Paragraph 0052-0053; 0089, (2017/08/31)

The invention relates to a method for preparing propane diamine by taking propylene glycol and liquid ammonia as raw materials. Propylene glycol and liquid ammonia are mixed in a certain ratio and are pumped into a reactor by virtue of a pump, and reaction is carried out in presence of a catalyst and hydrogen. The method for preparing the propane diamine by taking the propylene glycol and liquid ammonia as the raw materials has the advantages that a novel catalyst is adopted, catalytic performance is excellent, and long-time operation can be easily carried out; propylene glycol is subjected to hydroamination for producing a propane diamine product at lower reaction pressure, and reaction conditions are adjusted and changed, so that composition of the product can be flexibly adjusted and changed, selectivity of a target product is improved, a reaction process is simple, one-time investment of a production unit and production cost are reduced, a reaction product and a catalyst can be simply separated, and large-scale continuous industrial production can be easily realized.

METHOD FOR PRODUCING AMINES FROM SUGAR ALCOHOLS

-

Page/Page column 10, (2010/12/29)

The present invention relates to a process for preparing amines by reacting sugar alcohols with hydrogen and an aminating agent selected from the group of ammonia and primary and secondary amines in the presence of a catalyst at a temperature of from 100° C. to 400° C. and a pressure of from 1 to 40 MPa (from 10 to 400 bar). The catalyst preferably comprises one metal or a plurality of metals or one or more oxygen compounds of the metals of groups 8 and/or 9 and/or 10 and/or 11 of the Periodic Table of the Elements. The sugar alcohol is preferably obtained by hydrogenating the corresponding sugars. The invention further relates to the use of the reaction products as an additive in cement or concrete production and in other fields of use.

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