133405-86-4 Usage
Chemical class
1H-1,5-Benzodiazepine is a chemical compound belonging to the group of benzodiazepines.
Psychoactive properties
Benzodiazepines are known for their sedative, hypnotic, anxiolytic, and muscle relaxant properties.
Derivative
This compound is a derivative of benzodiazepine and is structurally related to widely used anti-anxiety and sedative drugs such as diazepam and alprazolam.
Molecular structure
The presence of the 2,3,4,5-tetrahydro-3-methyl group in the compound's molecular structure indicates a four-membered alicyclic ring with a methyl substituent at position 3.
Pharmacological properties
The presence of the tetrahydro-3-methyl group may contribute to the compound's pharmacological properties.
Pharmaceutical research and development
1H-1,5-Benzodiazepine, 2,3,4,5-tetrahydro-3-methylis of interest for pharmaceutical research and development due to its potential as a new therapeutic agent.
Treatment potential
This compound has the potential to be used in the treatment of anxiety and other central nervous system disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 133405-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,0 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133405-86:
(8*1)+(7*3)+(6*3)+(5*4)+(4*0)+(3*5)+(2*8)+(1*6)=104
104 % 10 = 4
So 133405-86-4 is a valid CAS Registry Number.
133405-86-4Relevant articles and documents
Synthesis of Benzimidazoles Containing a Fused Alicyclic Ring By Rhodium - Catalysed Hydroformylation of N-Alkenyl-1,2-diaminobenzenes
Anastasiou, Despina,Campi, Eva M.,Chaouk, Hassan,Jackson, W. Roy
, p. 7467 - 7478 (2007/10/02)
Rhodium-catalysed reactions of N-alkenyl-1,2-diaminobenzenes (3) with hydrogen and carbon monoxide give benzimidazoles containing a fused alicyclic ring ((8) and (9)) in excellent yields.In some cases intermediate bicyclic compounds can be isolated and the 1H and 13C n.m.r. spectra of one of these, the 3,4,5,6-tetrahydro-4-methyl-3H-1,6-benzodiazocine (6), shows evidence for unusual atropisomerism.
