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115706-39-3

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115706-39-3 Usage

Chemical class

Benzazepines
It belongs to a class of bicyclic compounds with a seven-membered nitrogen-containing ring fused to a six-membered benzene ring.

Molecular structure

Bicyclic ring system with an acetic acid side chain and a methyl group at the alpha carbon
The bicyclic ring system consists of a seven-membered azepine ring fused to a six-membered benzene ring. An acetic acid side chain is attached to the azepine ring, and a methyl group is present at the alpha carbon of the acetic acid side chain.

Psychoactive effects

Known for its psychoactive effects
The compound has been studied for its potential use in the treatment of various neurological and psychiatric disorders due to its psychoactive properties.

Potency

Potent inhibitor of dopamine and norepinephrine reuptake
It has shown significant inhibition of dopamine and norepinephrine reuptake, which is a key mechanism in the treatment of certain neurological and psychiatric disorders.

Potential therapeutic applications

Treatment of depression, bipolar disorder, and attention-deficit hyperactivity disorder (ADHD)
Preclinical and clinical studies have shown promise for the compound in treating these conditions due to its effects on neurotransmitter reuptake.

Unique structure

Valuable for further research and development in neuroscience and psychiatry
The compound's unique molecular structure and pharmacological properties make it an interesting candidate for further research in the fields of neuroscience and psychiatry.

Check Digit Verification of cas no

The CAS Registry Mumber 115706-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,0 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115706-39:
(8*1)+(7*1)+(6*5)+(5*7)+(4*0)+(3*6)+(2*3)+(1*9)=113
113 % 10 = 3
So 115706-39-3 is a valid CAS Registry Number.

115706-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,2,3,4-tetrahydro-2-oxo-5H-benzazepin-1-yl)propionic acid

1.2 Other means of identification

Product number -
Other names 2-(2-Oxo-2,3,4,5-tetrahydro-benzo[b]azepin-1-yl)-propionic acid

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:115706-39-3 SDS

115706-39-3Downstream Products

115706-39-3Relevant articles and documents

Synthesis and Antileukemic Activity of Bismethyl>-Substituted Pyrroloisoquinolines, Pyrroloquinolines, Pyrroloisobenzazepines, and Pyrrolobenzazepines

Anderson, Wayne K.,Heider, Arvela R.,Raju, Natarajan,Yucht, Jeffery A.

, p. 2097 - 2102 (2007/10/02)

A series of bismethyl>-substituted pyrrole-fused tricyclic heterocycles were synthesized by using 1,3-dipolar cycloaddition reactions with a trifluoromethanesulfonate salt of an appropriate Resissert compound or with a mesoionic oxazolone intermediate.All of the bis(carbamates) were active in vivo against P388 lymphocytic leukemia with 5,6-dihydro-8-methoxy-1,2-bis(hydroxymethyl)pyrroloisoquinoline bis (3c) showing the highest level of activity.

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