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6,7,8,9-TETRAHYDRO-5H-IMIDAZO[1,2-A]AZEPINE is a heterocyclic compound characterized by a bicyclic structure that includes both imidazole and azepine rings. It is a white to off-white crystalline powder, which exhibits solubility in organic solvents. This versatile chemical is frequently utilized in pharmaceutical research as a fundamental building block for the creation of a variety of biologically active compounds.
Used in Pharmaceutical Research:
6,7,8,9-TETRAHYDRO-5H-IMIDAZO[1,2-A]AZEPINE is used as a building block for the synthesis of biologically active compounds due to its unique structure and properties.
Used in Antipsychotic Drug Development:
6,7,8,9-TETRAHYDRO-5H-IMIDAZO[1,2-A]AZEPINE is used as a potential antipsychotic agent, given its pharmacological profile and the ongoing research into its efficacy in treating mental health disorders.
Used in Anti-inflammatory and Analgesic Applications:
6,7,8,9-TETRAHYDRO-5H-IMIDAZO[1,2-A]AZEPINE is used as a compound with anti-inflammatory and analgesic properties, indicating its potential use in the development of medications for pain relief and reducing inflammation.
Used in Organometallic Chemistry:
6,7,8,9-TETRAHYDRO-5H-IMIDAZO[1,2-A]AZEPINE is used as a potential ligand in organometallic chemistry, highlighting its role in the synthesis and stabilization of organometallic complexes.
Used in Organic Synthesis:
6,7,8,9-TETRAHYDRO-5H-IMIDAZO[1,2-A]AZEPINE is used as a reagent in organic synthesis, contributing to the formation of new organic compounds and facilitating various chemical reactions.

5768-55-8

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5768-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5768-55-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,6 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5768-55:
(6*5)+(5*7)+(4*6)+(3*8)+(2*5)+(1*5)=128
128 % 10 = 8
So 5768-55-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-2-4-8-9-5-7-10(8)6-3-1/h5,7H,1-4,6H2

5768-55-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7,8,9-Tetrahydro-5H-imidazo[1,2-a]azepine

1.2 Other means of identification

Product number -
Other names 2,3,4,6,7,8,9,10-octahydropyrimido<1,2-a>azepino

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5768-55-8 SDS

5768-55-8Relevant academic research and scientific papers

Radical cyclisation onto imidazoles and benzimidazoles

Aldabbagh, Fawaz,Bowman, W. Russell

, p. 4109 - 4122 (2007/10/03)

New synthetic methodology has been developed for the synthesis of [1,2- a]fused imidazoles and benzimidazoles using intramolecular homolytic aromatic substitution. In the intramolecular substitution, N-(ω-alkyl) radicals are generated using Bu3SnH from N-(ω-phenylselanyl)alkyl side chains. Phenylselanyl groups are used as radical leaving groups to avoid problems in the N-alkylation of imidazoles and benzimidazoles. Arylsulfones for imidazoles, and phenylsulfides for benzimidazoles, are used at the leaving groups in the homolytic substitutions.

Radical cyclisation onto imidazoles and benzimidazoles

Aldabbagh, Fawaz,Bowman, W. Russell

, p. 3793 - 3794 (2007/10/03)

A new protocol for the synthesis of [1,2-a]-fused benzimidazoles and imidazoles has been developed using intramolecular homolytic aromatic substitution via ω-alkyl radicals generated from 1-(ω-benzeneselenylakyl)-2(benzenesulfenyl)- benzimidazoles and -2-(p-toluenesulfonyl)imidazoles.

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