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
1H-1,5-Benzodiazepine, 2,3,4,5-tetrahydro-3-methyl- 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
1H-1,5-Benzodiazepine, 2,3,4,5-tetrahydro-3-methyl- 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 academic research and scientific papers
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.
