5768-55-8 Usage
General Description
6,7,8,9-Tetrahydro-5H-imidazo[1,2-a]azepine is a heterocyclic compound with a bicyclic structure containing both imidazole and azepine rings. It is a white to off-white crystalline powder that is soluble in organic solvents. This chemical is commonly used in pharmaceutical research as a building block for the synthesis of various biologically active compounds. It has been studied for its potential as an antipsychotic agent and has also been investigated for its anti-inflammatory and analgesic properties. Additionally, 6,7,8,9-Tetrahydro-5H-imidazo[1,2-a]azepine has been explored as a potential ligand in organometallic chemistry and as a reagent in organic synthesis.
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
5768-55-8Relevant articles and documents
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.
Condensation of Lactams with 2-Aminoacetylaldehyde Diethyl Acetal. A One-Pot Synthesis of Bicyclic Imidazoles
Hua, Duy H.,Zhang, Fengqi,Chen, Jinshan,Robinson, Paul D.
, p. 5084 - 5087 (2007/10/02)
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