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1H-Indole-3-carboxaldehyde, 5-butyl-2-[4-(trifluoromethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

588671-37-8

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588671-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 588671-37-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,8,6,7 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 588671-37:
(8*5)+(7*8)+(6*8)+(5*6)+(4*7)+(3*1)+(2*3)+(1*7)=218
218 % 10 = 8
So 588671-37-8 is a valid CAS Registry Number.

588671-37-8SDS

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 5-butyl-2-[4-(trifluoromethyl)phenyl]-1H-indole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1H-Indole-3-carboxaldehyde,5-butyl-2-[4-(trifluoromethyl)phenyl]

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:588671-37-8 SDS

588671-37-8Upstream product

588671-37-8Downstream Products

588671-37-8Relevant academic research and scientific papers

Antimitotic activities of 2-phenylindole-3-carbaldehydes in human breast cancer cells

Kaufmann, Doris,Pojarova, Michaela,Vogel, Susanne,Liebl, Renate,Gastpar, Robert,Gross, Dietmar,Nishino, Tsuyuki,Pfaller, Tobias,von Angerer, Erwin

, p. 5122 - 5136 (2007)

Small molecules such as indoles are attractive as inhibitors of tubulin polymerization. Thus a number of 2-phenylindole-3-carbaldehydes with lipophilic substituents in both aromatic rings was synthesized and evaluated for antitumor activity in MDA-MB 231

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