74651-77-7

Basic information

• Product Name: (E)-N-((tert-Butoxycarbonyl)oxy)benziMidoyl cyanide
• Synonyms: (E)-N-((tert-Butoxycarbonyl)oxy)benziMidoyl cyanide;tert-butyl [(Z)-[cyano(phenyl)methylidene]amino] carbonate
• CAS NO: 74651-77-7
• Molecular Formula: C₁₃H₁₄N₂O₃
• Molecular Weight: 246.26186
• Mol File: 74651-77-7.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 324.1±25.0 °C(Predicted)
• Appearance: /
• Density: 1.08±0.1 g/cm3(Predicted)
• CAS DataBase Reference: (E)-N-((tert-Butoxycarbonyl)oxy)benziMidoyl cyanide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N-((tert-Butoxycarbonyl)oxy)benziMidoyl cyanide(74651-77-7)
• EPA Substance Registry System: (E)-N-((tert-Butoxycarbonyl)oxy)benziMidoyl cyanide(74651-77-7)

Safety Data

• Hazardous Substances Data: 74651-77-7(Hazardous Substances Data)

Usage

Description

(E)-N-((tert-Butoxycarbonyl)oxy)benzimidoyl cyanide is an organic compound characterized by its unique chemical structure, which features a cyanide group and a benzene ring with a tert-butoxycarbonyloxy and benzimidoyl functional groups. (E)-N-((tert-Butoxycarbonyl)oxy)benziMidoyl cyanide is known for its potential applications in various chemical and pharmaceutical processes due to its reactive nature and versatile functional groups.

Uses

Used in Chemical Synthesis:
(E)-N-((tert-Butoxycarbonyl)oxy)benzimidoyl cyanide is used as a key intermediate in the synthesis of various organic compounds. Its reactive functional groups allow for a wide range of chemical reactions, making it a valuable building block in the creation of complex molecules.
Used in Pharmaceutical Industry:
(E)-N-((tert-Butoxycarbonyl)oxy)benzimidoyl cyanide is used as a synthetic building block for the development of new pharmaceutical compounds. Its unique structure and reactivity can be exploited to create novel drug candidates with potential therapeutic applications.
Used in the Synthesis of Novel Magnetic Reusable Organocatalysts:
(E)-N-((tert-Butoxycarbonyl)oxy)benzimidoyl cyanide is used as a crucial component in the synthesis of novel magnetic reusable organocatalysts. These organocatalysts have potential applications in various chemical reactions, offering an efficient and environmentally friendly alternative to traditional catalysts. The incorporation of this compound into the organocatalyst structure enhances their performance and reusability, making them valuable tools in the field of catalysis.

Downstream Products

• 192330-11-3 (R)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid 
• 117499-16-8 bis(2-tert-butyloxycarbonylaminoethyl)amine 
• 174138-01-3 1,4-di-tert-butyl 1,4,7-triazonane-1,4-dicarboxylate 
• 183669-13-8 tert-butyl (1-hydroxy-3-(4-nitrophenyl)propan-2-yl)carbamate 
• 183004-94-6 3-S-(N-tert-butyloxyformamido)-[2R-hydroxy-1-[(4-aminophenylsulfonyl)(2-methylpropyl)]amino]-4-phenylbutane 
• 99207-32-6 4-(N-tert-Butyloxycarbonyl-N-methylamino)butanol 
• 33305-77-0 Boc-Phe(p-NO₂)-OH 
• 13734-41-3 t-Boc-L-valine 
• 58885-58-8 N-tert-butoxycarbonyl-3-aminopropanol 
• 135680-03-4 N-{4-[(4-aminobenzyl)phenyl]}carbamic acid 1,1-dimethylethyl ester 
• 69610-40-8 N-(tert-butoxycarbonyl)-L-prolinol 
• 131980-30-8 (S)-2-((tert-butoxycarbonyl)amino)-3-(3-cyanophenyl)propanoic acid 
• 56583-58-5 N-tert-butoxycarbonyl-3-(2-naphthyl)-L-alanine 
• 145149-55-9 3-{[(tert-butoxycarbonyl)amino]methyl}cyclohexanecarboxylic acid