291-69-0

Basic information

• Product Name: 1H-Azepine
• Synonyms: 1H-Azepine;Azatropilidene
• CAS NO: 291-69-0
• Molecular Formula: C₆H₇N
• Molecular Weight: 93.1265
• Mol File: 291-69-0.mol

Chemical Properties

• Boiling Point: 199.5°Cat760mmHg
• Flash Point: 79.9°C
• Appearance: /
• Density: 0.93g/cm³
• Vapor Pressure: 0.341mmHg at 25°C
• Refractive Index: 1.507
• CAS DataBase Reference: 1H-Azepine(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Azepine(291-69-0)
• EPA Substance Registry System: 1H-Azepine(291-69-0)

Safety Data

• Hazardous Substances Data: 291-69-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1H-Azepine is used as a building block for the synthesis of various pharmaceuticals due to its reactivity and versatility. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
1H-Azepine is used as a precursor in the production of agrochemicals, contributing to the development of new pesticides and other agricultural chemicals that can improve crop protection and yield.
Used in Organic Synthesis:
1H-Azepine is utilized as a versatile precursor in organic synthesis, enabling the creation of a wide range of chemical compounds for various applications, including but not limited to, the development of new materials, dyes, and other specialty chemicals.

InChI:InChI=1/C6H7N/c1-2-4-6-7-5-3-1/h1-7H

Upstream product

• 105-60-2 caprolactam 
• 5960-99-6 7-(5'-aminopentyl)-3,4,5,6-tetrahydro-2H-azepine 
• 75863-30-8 1H-Azepin-N-carbonsaeure-trimethylsilylester 
• 17870-94-9 N-methoxycarbonyl-1H-azepine 
• 75863-31-9 Azepine-1-carboxylic acid 

Downstream Products

• 20646-53-1 N-Methansulfonyl-1H-azepin 

Relevant articles and documents

Luminescent element material, luminescent element, ethylene derivative having n-containing 7-membered ring, and benzoazepine derivative

Disclosed are a luminescent element material comprising a polymer having a partial structure represented by formula (I) and a luminescent element usin the same.

Tricyclic 2,3,4,5-tetrahydro-1H-3-benzapines

Tricyclic benzazepines having the general formula STR1 wherein A together with the α- and β-marked carbon atoms is a cyclopentene, cyclohexene, furan, dihydrofuran, pyran, dihydropyran, thiophene, oxazole, pyrrole, pyrroline, tetrahydropyridine or dioxole ring, R1 is H or alkyl, R2 and R3 independently are H, alkoxy, halogen, nitro, cyano or hydroxy, or R2 and R3 together may form a furan, dihydrofuran, cyclopentene or dioxole ring and R4 is H, alkoxy, nitro, cyano, hydroxy or halogen, or a pharmaceutically acceptable salt thereof, are useful in treatment of certain disorders in the central nervous system, e.g., psychosis, pain, depression, sleep disturbances, dyskinesia, Parkinson's disease, stroke.

Process for the preparation of Schiff's bases

A process for the preparation of Schiff's bases which contain amino groups, of the formula STR1 wherein n is 3 to 12, by reacting cyclic lactams of the formula STR2 wherein n is 3 to 12, or of their ring-opened polymers of the formula STR3 wherein n is 3 to 12 and m is 1 to 100,000, with inorganic bases at elevated temperature, the reaction being carried out in the presence of inert, high-boiling suspending agents.