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(3,4,5,6-TETRAHYDRO-2H-AZEPIN-7-YLAMINO)ACETIC ACID, also known as THAZAA, is a chemical compound with potential pharmaceutical applications. It is a small molecule that acts as a GABA receptor agonist, affecting the GABAergic system in the brain. THAZAA has been studied for its potential use in treating anxiety, depression, and other psychiatric disorders, as well as for its potential as a pain reliever. THAZAA may have the ability to modulate the activity of neurotransmitters in the brain, leading to potential therapeutic effects. Its pharmacological properties make it a promising candidate for further research and development in the pharmaceutical industry.

90152-88-8

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90152-88-8 Usage

Uses

Used in Pharmaceutical Industry:
(3,4,5,6-TETRAHYDRO-2H-AZEPIN-7-YLAMINO)ACETIC ACID is used as a GABA receptor agonist for its potential therapeutic effects in treating anxiety, depression, and other psychiatric disorders.
(3,4,5,6-TETRAHYDRO-2H-AZEPIN-7-YLAMINO)ACETIC ACID is used as a potential pain reliever for its ability to modulate the activity of neurotransmitters in the brain.

Check Digit Verification of cas no

The CAS Registry Mumber 90152-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90152-88:
(7*9)+(6*0)+(5*1)+(4*5)+(3*2)+(2*8)+(1*8)=118
118 % 10 = 8
So 90152-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H14N2O2/c11-8(12)6-10-7-4-2-1-3-5-9-7/h1-6H2,(H,9,10)(H,11,12)

90152-88-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4,5,6-tetrahydro-2H-azepin-7-ylamino)acetic acid

1.2 Other means of identification

Product number -
Other names N-(3'H-4',5',6',7'-tetrahydroazepin-2'-yl)aminoacetic 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:90152-88-8 SDS

90152-88-8Downstream Products

90152-88-8Relevant academic research and scientific papers

Hydroxylation of 5H-3-Oxo-2,3,6,7,8,9-hexahydroimidazoazepine Derivatives by Molecular Oxygen

Campagna, Francesco,Carotti, Angelo,Casini, Giovanni

, p. 1973 - 1977 (2007/10/02)

O-Methylcaprolactim 3 reacts in hot dimethylsulfoxide with α-amino acids 4 to give 5H-3-oxo-2,3,6,7,8,9-hexahydroimidazoazepines 6 and, unexpectedly, hydroxylated derivatives 7a,c and 8c.The structures of the hydroxylated compounds have been elucid

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