32063-84-6

Basic information

• Product Name: 2-Cyano-1-tert-butyl-aziridin
• CAS NO: 32063-84-6
• Molecular Weight: 124.186
• Mol File: 32063-84-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Cyano-1-tert-butyl-aziridin(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyano-1-tert-butyl-aziridin(32063-84-6)
• EPA Substance Registry System: 2-Cyano-1-tert-butyl-aziridin(32063-84-6)

Safety Data

• Hazardous Substances Data: 32063-84-6(Hazardous Substances Data)

Upstream product

• 1104196-24-8 t-butyl-3-N-chloroaminopropionitrile 
• 31367-72-3 1-cyanovinyl methanesulfonate 
• 75-64-9 tert-butylamine 
• 4554-16-9 2,3-dibromopropionitrile 

Downstream Products

• 84269-67-0 (α-iminobenzyl)-2 t-butyl-1 aziridine 

Relevant articles and documents

Synthesis of substituted aziridines via intramolecular reactions of β-N-chloroethylamino carbanions

Simple and efficient method of synthesis of 2-alkoxycarbonyl, 2-cyano, 2-phenylsulfonyl N-alkylaziridines was elaborated via intramolecular nucleophiles substitution of chloride in 1-N-chloro-2-alkoxycarbonyl (cyano, phenylsulfonyl) ethyl amines. These su

REACTION OF HYDROGEN FLUORIDE IN PYRIDINE SOLUTION WITH CIS-CYANO-2 AND CIS-AMIDO-2-AZIRIDINES. PREPARATION OF β-FLUORO α-AMINO ACIDS AND ESTERS BY MEANS OF ACID HYDROLYSIS AND ALCOHOLYSIS OF β-FLUORO-α-AMINONITRILES AND/OR β-FLUORO-α-AMINO ACID AMIDES

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N-Substituted aziridine-2-carboxylic acid derivatives for immuno stimulation

Aziridine-2-carboxylic acid derivatives of the formula STR1 wherein X is a carboxyl, nitrile, alkoxycarbonyl or carbamoyl group, and R and R1 are various organic radicals, or pharmacologically acceptable salts thereof, exhibit marked immunostimulant activity, especially in conjunction with added chemotherapeutic agents such as a penicillin, a cephalosporin, a nitrofuran or chloramphenicol. Those compounds are new where X is a cyano group or an alkoxycarbonyl radical and R1 is a hydrogen atom, but R' is not an unsubstituted alkyl radical or an alkyl radical substituted by hydroxyl, alkoxy, dialkylamino, phenyl, 4-chlorophenyl or 4-methoxyphenyl or a vinyl radical substituted by a phenyl or methyl radical, or a cycloalkyl radical, a phenyl a 4-chlorophenyl, a 4-methoxyphenyl, an s-triazinyl or a pyridinyl radical; or where X is a carbamoyl group and R1 is a hydrogen atom, R' is not an unsubstituted cyclohexyl, alkyl or benzyl radical; or where X is a cyano group or an alkoxycarbonyl radical and R1 is a phenyl radical, R' is not an isopropyl, cyclohexyl, phenyl, benzyl or p-chlorobenzyl radical; or where R1 is a methyl radical, R1 is not a benzyl, p-chloro- or p- methoxybenzyl radical.