ChemicalBook Product Catalog Chemical Reagents Organic reagents Cyanide / nitrile 3-(BENZYLAMINO)PROPIONITRILE

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 Structure
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.)
Fp >230 °F
storage temp. Refrigerator
solubility Soluble in DMSO.
pka7.29±0.19(Predicted)
form Liquid
color Clear Colorless
Specific Gravity1.024
CAS DataBase Reference706-03-6
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 Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
3-(BENZYLAMINO)PROPIONITRILE Usage And Synthesis
Chemical PropertiesCLEAR COLOURLESS LIQUID
Uses3-(BenzylaMino)propionitrile is used in the michael addition of primary and secondary amines to acrylonitrile catalyzed by lipases.
Uses3-(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
Application3-(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 Description3-(Benzylamino)propionitrile undergoes aza-type Michael reaction with 1-hydroxymethyl-5-methyl-1H-pyrazole-3-carboxylic acid ethyl ester under mild conditions.
3-(BENZYLAMINO)PROPIONITRILE Preparation Products And Raw materials
6-(4-FLUOROPHENYL)-1,2-DIHYDRO-2-OXOPYRIDINE-3-CARBONITRILE 1-(2,6-DICHLOROBENZYL)-2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 1-(2,4-DICHLOROBENZYL)-6-(4-FLUOROPHENYL)-2-OXO-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 3-(BENZYLAMINO)PROPIONITRILE 1-(4-CHLOROBENZYL)-6-(DIMETHOXYMETHYL)-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 N-(2-CYANOETHYL)-PHTHALIMIDE 3-(2-oxobenzo[cd]indol-1(2H)-yl)propanenitrile N1,N1-DI(2-CYANOETHYL)-4-CHLORO-3-NITROBENZAMIDE 1-(2-CHLOROBENZYL)-2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 1-(4-METHYLBENZYL)-2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 1,3-DIBENZYL-5-CYANOHEXAHYDROPYRIMIDINE 1-(2-CHLORO-6-FLUOROBENZYL)-6-(4-FLUOROPHENYL)-2-OXO-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 6-(4-FLUOROPHENYL)-2-OXO-1-[3-(TRIFLUOROMETHYL)BENZYL]-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 1-(3,4-DICHLOROBENZYL)-6-(4-FLUOROPHENYL)-2-OXO-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 1-METHYL-4-(METHYLSULFANYL)-2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 6-(4-CHLOROPHENYL)-1-(3,4-DICHLOROBENZYL)-2-OXO-1,2-DIHYDRO-3-PYRIDINECARBONITRILE 1-(3-CHLOROBENZYL)-2-OXO-6-PHENYL-1,2-DIHYDRO-3-PYRIDINECARBONITRILE
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