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1H-Indole, 5-(phenylmethoxy)-2-(1H-pyrrol-2-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

569337-40-2

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569337-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 569337-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,9,3,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 569337-40:
(8*5)+(7*6)+(6*9)+(5*3)+(4*3)+(3*7)+(2*4)+(1*0)=192
192 % 10 = 2
So 569337-40-2 is a valid CAS Registry Number.

569337-40-2SDS

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 5-phenylmethoxy-2-(1H-pyrrol-2-yl)-1H-indole

1.2 Other means of identification

Product number -
Other names 5-benzyloxy-2-(1H-pyrrol-2-yl)-1H-indole

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:569337-40-2 SDS

569337-40-2Relevant academic research and scientific papers

Synthesis and biological activities of isogranulatimide analogues

Hugon, Bernadette,Anizon, Fabrice,Bailly, Christian,Golsteyn, Roy M.,Pierre, Alain,Leonce, Stephane,Hickman, John,Pfeiffer, Bruno,Prudhomme, Michelle

, p. 5965 - 5980 (2008/03/15)

The synthesis of new isogranulatimide analogues, their inhibitory activities toward the Checkpoint 1 kinase (Chk1), and their in vitro cytotoxicities toward four tumor cell lines (one murine L1210 leukemia, and three human cell lines: DU145 prostate carci

Synthesis of isogranulatimide analogues possessing a pyrrole moiety instead of an imidazole heterocycle

Hugon, Bernadette,Pfeiffer, Bruno,Renard, Pierre,Prudhomme, Michelle

, p. 3927 - 3930 (2007/10/03)

An efficient four step synthesis from commercial indoles of isogranulatimide analogues is reported. In the new compounds, the imidazole moiety is replaced by a pyrrole unit, the indole part is substituted or not in 5-position and the nitrogen of the imide moiety bears or not a methyl substituent.

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