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149231-54-9

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149231-54-9 Usage

Chemical compound

6-CHLORO-3-INDOLYL ACETATE

Structure

6-chlorinated indole ring attached to an acetate group

Usage

Reagent in organic synthesis, particularly in preparation of indole derivatives

Properties

Potential anti-inflammatory and anti-cancer properties

Applications

Inhibition of certain cancer cell growth, reduction of inflammation in animal models

Research

Used in study of plant growth and development, mimics action of plant hormone auxin

Check Digit Verification of cas no

The CAS Registry Mumber 149231-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,2,3 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149231-54:
(8*1)+(7*4)+(6*9)+(5*2)+(4*3)+(3*1)+(2*5)+(1*4)=129
129 % 10 = 9
So 149231-54-9 is a valid CAS Registry Number.

149231-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-acetyl-6-chloro-indol-3-ol

1.2 Other means of identification

Product number -
Other names 6-chloro-3-indolyl-1-acetate

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:149231-54-9 SDS

149231-54-9Downstream Products

149231-54-9Relevant articles and documents

N-ARYLSULFONYL-3-AMINOALKOXYINDOLES

-

Page 56, (2008/06/13)

The present invention describes substituted 3-Aminoalkoxyindoles, compounds of the general formula (I), its stereoisomers, its radioisotopes, its geometric forms, its N-oxides, its polymorphs, its pharmaceutically acceptable salts, its pharmaceutically acceptable solvates, its useful bio-active metabolites and any suitable combination of the above. The invention also discloses the processes for preparing such compounds of the general formula (I), its stereoisomers, its radioisotopes, its geometric forms, its N-oxides, its polymorphs, its pharmaceutically acceptable salts, its pharmaceutically acceptable solvates, its useful bio-active metabolites and also includes any suitable combination of the above. Further described are various methods of administering these compounds of general formula (I), i.e. pharmaceutically acceptable dosage forms, their composition and their use in either therapy or diagnosis.

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