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6547-98-4

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6547-98-4 Usage

Molecular weight

189.21 g/mol

Structure

A derivative of 1,2-propanediol (propylene glycol) containing an indole ring.

Usage

Commonly used in organic synthesis and pharmaceutical research.

Biological activities

Known for antiproliferative and anticancer properties.

Potential applications

Studied for its potential in drug development and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 6547-98-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6547-98:
(6*6)+(5*5)+(4*4)+(3*7)+(2*9)+(1*8)=124
124 % 10 = 4
So 6547-98-4 is a valid CAS Registry Number.

6547-98-4SDS

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 3-indol-3-yl-propane-1,2-diol

1.2 Other means of identification

Product number -
Other names 3-Indol-3-yl-propan-1,2-diol

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:6547-98-4 SDS

6547-98-4Relevant articles and documents

Synthesis and biological activities of indolactone-V, the lactone analogue of the tumor promoter (-)-indolactam-V.

Nakagawa,Irie,Nakamura,Ohigashi,Hayashi

, p. 1415 - 1417 (1997)

The tumor promoter (-)-indolactam-V (1) exists in two stable conformers (twist and sofa) due to isomerization of the amide group. Indolactone-V (2), the lactone analogue of 1, has been synthesized to investigate the effects of the amide group on its conformation and biological activities. Indolactone-V (2) existed only as the inactive sofa-like conformer, indicating that the amide group of 1 plays a critical role in formation of the active twist conformation.

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