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1H-Indole-2-methanol, 6-methyl-4-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65752-12-7

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65752-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65752-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,5 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65752-12:
(7*6)+(6*5)+(5*7)+(4*5)+(3*2)+(2*1)+(1*2)=137
137 % 10 = 7
So 65752-12-7 is a valid CAS Registry Number.

65752-12-7SDS

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 (4-(benzyloxy)-6-methyl-1H-indol-2-yl)methanol

1.2 Other means of identification

Product number -
Other names 4-Benzyloxy-2-hydroxymethyl-6-methylindol

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:65752-12-7 SDS

65752-12-7Relevant academic research and scientific papers

The first potent inhibitor of mammalian group X secreted phospholipase A2: Elucidation of sites for enhanced binding

Smart, Brian P.,Oslund, Rob C.,Walsh, Laura A.,Gelb, Michael H.

, p. 2858 - 2860 (2007/10/03)

Using the X-ray structure of human group X secreted phospholipase A 2 (hGX), we carried out structure-based design of indole-based inhibitors and prepared the compounds using a new synthetic route. The most potent compound inhibited hGX and the mouse orthologue with an IC50 of 75 nM. This compound is the most potent hGX inhibitor reported to date and was also found to inhibit a subset of the other mouse and human SPLA 2S.

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