3-(BENZYLAMINO)PROPIONITRILE
3-(BENZYLAMINO)PROPIONITRILE Basic information
- Product Name:
- 3-(BENZYLAMINO)PROPIONITRILE
- Synonyms:
-
- 3-(BENZYLAMINO)PROPIONITRILE
- 3-(BENZYLAMINO)PROPIONITRILE, 97+%
- 3-[(Phenylmethyl)amino]propanenitrile
- N-(2-Cyanoethyl)benzenemethanamine
- β-(Benzylamino)propionitrile
- 3-(Benzylamino)propionitrile 97%
- Propanenitrile, 3-[(phenylmethyl)amino]-
- CAS:
- 706-03-6
- MF:
- C10H12N2
- MW:
- 160.22
- EINECS:
- 211-890-7
- Product Categories:
-
- C10 to C27
- Cyanides/Nitriles
- Nitrogen Compounds
- Mol File:
- 706-03-6.mol
3-(BENZYLAMINO)PROPIONITRILE Chemical Properties
- Melting point:
- 70 °C
- Boiling point:
- 276.13°C (rough estimate)
- Density
- 1.024 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.5308(lit.)
- Flash point:
- >230 °F
- storage temp.
- Refrigerator
- solubility
- Soluble in DMSO.
- form
- Liquid
- pka
- 7.29±0.19(Predicted)
- color
- Clear Colorless
- Specific Gravity
- 1.024
- CAS DataBase Reference
- 706-03-6
Safety Information
- Hazard Codes
- Xn,Xi
- Risk Statements
- 20/21/22-36/37/38
- Safety Statements
- 26-37/39
- RIDADR
- UN3276
- WGK Germany
- 3
- HazardClass
- 6.1
- PackingGroup
- III
- HS Code
- 29269095
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
3-(BENZYLAMINO)PROPIONITRILE Usage And Synthesis
Chemical Properties
CLEAR COLOURLESS LIQUID
Uses
3-(Benzylamino)propionitrile was used as starting reagent in the synthesis of:
- (3R,4S)-1-benzyl-4-phenylpyrrolidine-3-carboxylic acid, key chiral building block for synthesis of biologically active compounds
- 1-{[benzyl-(2-cyano-ethyl)-amino]-methyl}-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester
- 3-[benzyl-(3,5-dimethyl-pyrazol-1-ylmethyl)-amino]-propionitrile
Uses
3-(BenzylaMino)propionitrile is used in the michael addition of primary and secondary amines to acrylonitrile catalyzed by lipases.
Application
3-(Benzylamino)propionitrile was used as starting reagent in the synthesis of:
(3R,4S)-1-benzyl-4-phenylpyrrolidine-3-carboxylic acid, key chiral building block for synthesis of biologically active compounds
1-{[benzyl-(2-cyano-ethyl)-amino]-methyl}-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester
3-[benzyl-(3,5-dimethyl-pyrazol-1-ylmethyl)-amino]-propionitrile
General Description
3-(Benzylamino)propionitrile undergoes aza-type Michael reaction with 1-hydroxymethyl-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester under mild conditions.
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3-(BENZYLAMINO)PROPIONITRILE(706-03-6)Related Product Information
- 3-(BENZYLAMINO)PROPIONITRILE
- 1,3-DIBENZYL-5-CYANOHEXAHYDROPYRIMIDINE
- 1-Benzhydrylazetane-3-carbonitrile
- 3-(4-CHLORO-BENZYLAMINO)-PROPIONITRILE
- Propionitrile
- 6-(4-FLUOROPHENYL)-1,2-DIHYDRO-2-OXOPYRIDINE-3-CARBONITRILE
- N-(2-CYANOETHYL)-PHTHALIMIDE
- 2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE
- 6-(4-CHLOROPHENYL)-1-(3,4-DICHLOROBENZYL)-2-OXO-1,2-DIHYDRO-3-PYRIDINECARBONITRILE
- 4-(METHYLTHIO)-6-OXO-2-PHENYL-1,6-DIHYDROPYRIMIDINE-5-CARBONITRILE
- 1-(3-CHLOROBENZYL)-2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE
- 1-(3,4-DICHLOROBENZYL)-6-(4-FLUOROPHENYL)-2-OXO-1,2-DIHYDRO-3-PYRIDINECARBONITRILE
- 1-[[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL](METHYL)AMINO]-3-(4-FLUOROBENZYL)-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINECARBONITRILE
- N1,N1-DI(2-CYANOETHYL)-4-CHLORO-3-NITROBENZAMIDE
- 6-(4-FLUOROPHENYL)-2-OXO-1-[3-(TRIFLUOROMETHYL)BENZYL]-1,2-DIHYDRO-3-PYRIDINECARBONITRILE
- 1-(2-CHLOROBENZYL)-2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE
- 1-(4-CHLOROBENZYL)-6-(DIMETHOXYMETHYL)-2-OXO-1,2-DIHYDRO-3-PYRIDINECARBONITRILE
- 1-METHYL-4-(METHYLSULFANYL)-2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE