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98323-83-2

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  • 3-[4-(3,6-DIHYDRO-4-PHENYL-1(2H)-PYRIDINYL)BUTYL]-1H-INDOLE-5-CARBOXYLIC ACID HYDROCHLORIDE

    Cas No: 98323-83-2

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98323-83-2 Usage

Uses

Carmoxirole is a selective, peripherally acting D2-like agonist.

Definition

ChEBI: An indolecarboxylic acid that is indole-5-carboxylic acid bearing an additional 4-(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)butyl substituent at position 3. Selective, peripherally acting dopamine D2 receptor agonist. Modulates noradren lin release and sympathetic activation. Displays antihypertensive properties in vivo.

Biological Activity

Selective, peripherally acting dopamine D 2 receptor agonist. Modulates noradrenalin release and sympathetic activation. Displays antihypertensive properties in vivo .

Check Digit Verification of cas no

The CAS Registry Mumber 98323-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,2 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 98323-83:
(7*9)+(6*8)+(5*3)+(4*2)+(3*3)+(2*8)+(1*3)=162
162 % 10 = 2
So 98323-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C24H26N2O2/c27-24(28)20-9-10-23-22(16-20)21(17-25-23)8-4-5-13-26-14-11-19(12-15-26)18-6-2-1-3-7-18/h1-3,6-7,9-11,16-17,25H,4-5,8,12-15H2,(H,27,28)

98323-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name carmoxirole

1.2 Other means of identification

Product number -
Other names 3-[4-(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)butyl]-1H-indole-5-carboxylic 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:98323-83-2 SDS

98323-83-2Downstream Products

98323-83-2Relevant articles and documents

A new synthesis of indole 5-carboxylic acids and 6-hydroxy-indole-5- carboxylic acids in the preparation of an o-hydroxylated metabolite of vilazodone

Heinrich, Timo,Boettcher, Henning

, p. 2681 - 2684 (2007/10/03)

A major metabolite of the potential antidepressant vilazodone formed in rat, dog, monkey and human liver microsomes is the 5-cyano-6-hydroxy-1H-indole derivative. For the construction of the salicyl-like substituted indole we adapted a synthesis of carmox

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