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80714-55-2

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80714-55-2 Usage

General Description

(S)-1-chloro-3-(1H-imidazol-4-yl)propan-2-amine, also known as R-CHIM, is a chemical compound with the molecular formula C6H10ClN3. It is an amine derivative of imidazole, and is commonly used in pharmaceutical research and drug development. (S)-1-chloro-3-(1H-iMidazol-4-yl)propan-2-aMine is known to have an affinity for the GABA-A receptor, and has shown potential as a treatment for anxiety and stress-related disorders. Additionally, it is being studied for its potential role in reducing symptoms of withdrawal from alcohol and other substances. Its activity on the central nervous system makes it a target for further investigation into its potential therapeutic uses.

Check Digit Verification of cas no

The CAS Registry Mumber 80714-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,1 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80714-55:
(7*8)+(6*0)+(5*7)+(4*1)+(3*4)+(2*5)+(1*5)=122
122 % 10 = 2
So 80714-55-2 is a valid CAS Registry Number.

80714-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-Chloro-3-(1H-imidazol-5-yl)-2-propanamine

1.2 Other means of identification

Product number -
Other names SYSMEHFRWGKPV-NH2

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:80714-55-2 SDS

80714-55-2Upstream product

80714-55-2Relevant articles and documents

Histamine analogues. 32nd communication: synthesis and pharmacology of sopromidine, a potent and stereoselective isomer of the achiral H2-agonist impromidine

Elz, Sigurd,Gerhard, Guenter,Schunack, Walter

, p. 259 - 262 (2007/10/02)

Synthesis and pharmacology of sopromidine ((R)-7) and (S)-7, 2 position isomers of impromidine derived from the enantiomeric α-methylhistamines, are reported.The enantiomers of 7 show high stereoselectivity at the atrial H2-receptor of the guinea-pig. (R)-7 is revealed to be a full H2-agonist with 7.4-fold potency relative to histamine, while (S)-7 is a competitive H2-antagonist. chiral H2-agonists / histamine H2-receptor / impromidine analogues / α-methylhistamine

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