313673-94-8 Usage
General Description
7-Chloro-2,3,4,5-tetrahydro-1H-benzo[b]azepine hydrochloride is a chemical compound with potential anxiolytic and antidepressant effects. It belongs to the class of heterocyclic compounds and is structurally related to tricyclic antidepressants. 7-CHLORO-2,3,4,5-TETRAHYDRO-1H-BENZO[B]AZEPINE HYDROCHLORIDE acts by modulating the levels of certain neurotransmitters in the brain, such as serotonin and norepinephrine, which are known to regulate mood and anxiety. It is commonly used in the pharmaceutical industry for the production of medication for the treatment of anxiety and mood disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 313673-94-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,6,7 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 313673-94:
(8*3)+(7*1)+(6*3)+(5*6)+(4*7)+(3*3)+(2*9)+(1*4)=138
138 % 10 = 8
So 313673-94-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12ClN/c11-9-4-5-10-8(7-9)3-1-2-6-12-10/h4-5,7,12H,1-3,6H2
313673-94-8Relevant articles and documents
Tetrahydroquinoline-Capped Histone Deacetylase 6 Inhibitor SW-101 Ameliorates Pathological Phenotypes in a Charcot-Marie-Tooth Type 2A Mouse Model
Shen, Sida,Picci, Cristina,Ustinova, Kseniya,Benoy, Veronick,Kutil, Zsófia,Zhang, Guiping,Tavares, Maurício T.,Pavlí?ek, Ji?í,Zimprich, Chad A.,Robers, Matthew B.,Van Den Bosch, Ludo,Ba?inka, Cyril,Langley, Brett,Kozikowski, Alan P.
, p. 4810 - 4840 (2021/05/07)
Histone deacetylase 6 (HDAC6) is a promising therapeutic target for the treatment of neurodegenerative disorders. SW-100 (1a), a phenylhydroxamate-based HDAC6 inhibitor (HDAC6i) bearing a tetrahydroquinoline (THQ) capping group, is a highly potent and sel
Synthesis of tetrahydrobenzazepinesulfonamides and their rearrangement to diarylsulfones
Ren, Hui,Zanger, Murray,McKee, James R.
, p. 355 - 363 (2007/10/03)
A new class of diarylsulfones, in which tetrahydrobenzazepine comprises one of the aromatic moieties, has been synthesized via the acid-catalyzed rearrangement of several substituted benzazepinesulfonamides. The rearrangement is normally ortho but in at l