362509-57-7

Basic information

• Product Name: BENZYL 2-METHYL-2,3,4,7-TETRAHYDRO-1H-AZEPINE-1-CARBOXYLATE
• Synonyms: BENZYL 2-METHYL-2,3,4,7-TETRAHYDRO-1H-AZEPINE-1-CARBOXYLATE
• CAS NO: 362509-57-7
• Molecular Formula: C₁₅H₁₉NO₂
• Molecular Weight: 245.31686
• Mol File: 362509-57-7.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZYL 2-METHYL-2,3,4,7-TETRAHYDRO-1H-AZEPINE-1-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYL 2-METHYL-2,3,4,7-TETRAHYDRO-1H-AZEPINE-1-CARBOXYLATE(362509-57-7)
• EPA Substance Registry System: BENZYL 2-METHYL-2,3,4,7-TETRAHYDRO-1H-AZEPINE-1-CARBOXYLATE(362509-57-7)

Safety Data

• Hazardous Substances Data: 362509-57-7(Hazardous Substances Data)

Upstream product

• 362509-54-4 allyl(1-methylpent-4-enyl)carbamic acid benzyl ester 
• 109-49-9 5-Hexen-2-one 
• 35021-88-6 allyl(1-methylpent-4-enylidene)amine 
• 362509-50-0 allyl-(1-methylpent-4-enyl)amine 

Downstream Products

• 362507-64-0 Benzofuran-2-carboxylic acid {(S)-3-methyl-1-[(4R,7R)-7-methyl-3-oxo-1-(pyridine-2-sulfonyl)-azepan-4-ylcarbamoyl]-butyl}-amide 
• 362505-84-8 Relacatib 
• 362507-64-0 Benzofuran-2-carboxylic acid {(S)-3-methyl-1-[(4R,7S)-7-methyl-3-oxo-1-(pyridine-2-sulfonyl)-azepan-4-ylcarbamoyl]-butyl}-amide 
• 362507-64-0 Benzofuran-2-carboxylic acid {(S)-3-methyl-1-[(4S,7S)-7-methyl-3-oxo-1-(pyridine-2-sulfonyl)-azepan-4-ylcarbamoyl]-butyl}-amide 
• 403700-44-7 5-((S)-2-tert-butoxycarbonylamino-4-methylpentanoylamino)-6-hydroxy-2-methylazepane-1-carboxylic acid benzyl ester 

Relevant articles and documents

Semiheterogeneous Purification Protocol for the Removal of Ruthenium Impurities from Olefin Metathesis Reaction Products Using an Isocyanide Scavenger

A low-waste, time-economical, and scalable semiheterogeneous purification protocol for the removal of ruthenium residues from olefin metathesis (OM) reactions has been developed. It is based on the non-covalent immobilization of the commercially available

Bis(Cyclic Alkyl Amino Carbene) Ruthenium Complexes: A Versatile, Highly Efficient Tool for Olefin Metathesis

The state-of-the-art in olefin metathesis is application of N-heterocyclic carbene (NHC)-containing ruthenium alkylidenes for the formation of internal C=C bonds and of cyclic alkyl amino carbene (CAAC)-containing ruthenium benzylidenes in the production of terminal olefins. A straightforward synthesis of bis(CAAC)Ru indenylidene complexes, which are highly effective in the formation of both terminal and internal C=C bonds at loadings as low as 1 ppm, is now reported.

Structure activity relationships of 5-, 6-, and 7-methyl-substituted azepan-3-one cathepsin K inhibitors

The syntheses, in vitro characterizations, and rat and monkey in vivo pharmacokinetic profiles of a series of 5-, 6-, and 7-methyl-substituted azepanone-based cathepsin K inhibitors are described. Depending on the particular regiochemical substitution and