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ChemicalBook--->CAS DataBase List--->540-61-4

540-61-4

540-61-4 Structure

540-61-4 Structure
IdentificationBack Directory
[Name]

AMINOACETONITRILE
[CAS]

540-61-4
[Synonyms]

SKL069
H2NCH2CN
Glycinenitrile
Glycinonitrile
Cyanomethylamine
AMINOACETONITRILE
amino-acetonitril
Aminocyanomethane
2-Aminoacetonitrile
Acetonitrile, amino-
2-azanylethanenitrile
Aminoacetonitrile ,95%
AMinoacetonitrile >=98%
alpha-Aminoacetonitrile
aminoacetonitrilefreebase
Acetonitrile, amino- (8CI,9CI)
Cyanomethylamine, Glycinonitrile
[EINECS(EC#)]

208-751-8
[Molecular Formula]

C2H4N2
[MDL Number]

MFCD00078890
[MOL File]

540-61-4.mol
[Molecular Weight]

56.07
Chemical PropertiesBack Directory
[Melting point ]

101 °C
[Boiling point ]

bp15 58° (partial decompn)
[density ]

0.7789 (rough estimate)
[refractive index ]

1.4180 (estimate)
[storage temp. ]

−20°C
[form ]

liquid
[pka]

5.34(at 25℃)
[CAS DataBase Reference]

540-61-4
[NIST Chemistry Reference]

NCCH2NH2(540-61-4)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-40
[Safety Statements ]

23-36
[RIDADR ]

NA 1993 / PGIII
[WGK Germany ]

3
[RTECS ]

AL7750000
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methylenaminoacetonitrile
[Preparation Products]

Glycine-->5-Amino-1,2,3-thiadiazole-->Glycinamide-->N,N-Diethylethylenediamine-->2-Aminoimidazole-->N-Aminoethylpiperazine-->2-Benzylidenemalonaldehyde-->Momelotinib-->3-BENZYLPYRIDINE-->Cathepsin Inhibitor 1-->3-Isoquinolinecarbonitrile-->5-Thiazolamine, 2-methyl--->2-(1H-PYRROL-1-YL)ACETONITRILE-->4-AMino-3-benzoyl-2-Methylpyrrole-->ETHYL 4-AMINO-1H-IMIDAZOLE-2-CARBOXYLATE-->5,6,7,8,9,10-hexahydrocycloocta[b]pyridine
Hazard InformationBack Directory
[Uses]

Aminoacetonitrile is used in preparation of the Heterocyclic compounds and their medical applications.
[Production Methods]

Aminoacetonitrile is readily obtained as an aqueous solution by reacting an aqueous solution of glycolonitrile with liquid ammonia. The solution is stabilized by lowering the pH with small amounts of sulfuric acid. Aminoacetonitrile can also be isolated as the hydrochloride or sulfate. Aminoacetonitrile is usually further hydrolyzed by sodium hydroxide to the sodium salt of glycine, which in turn is neutralized to glycine.
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