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1H-Indole-6-methanol,4-methoxy-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

791807-50-6

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791807-50-6 Usage

Derivative of indole

A naturally occurring compound found in certain plants and animals

Functional groups

Methanol and methoxy groups attached to the indole ring

Industrial applications

Used in the production of pharmaceuticals, fragrances, and dyes

Biological and medicinal properties

Potential as an anti-cancer agent, but further research is needed to fully understand its mechanisms and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 791807-50-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,8,0 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 791807-50:
(8*7)+(7*9)+(6*1)+(5*8)+(4*0)+(3*7)+(2*5)+(1*0)=196
196 % 10 = 6
So 791807-50-6 is a valid CAS Registry Number.

791807-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxy-1H-indol-6-yl)methanol

1.2 Other means of identification

Product number -
Other names (4-Methoxy-1H-indol-6-yl)-methanol

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:791807-50-6 SDS

791807-50-6Relevant academic research and scientific papers

A synthetic approach toward the proposed tetracyclic aziridinomitosene derived from FK317

Kim, Musong,Vedejs, Edwin

, p. 7262 - 7265 (2004)

A synthesis of the FK317 derivative 25 is described using internal Michael addition. Tin-lithium exchange of the deuterated stannylaziridine 18 generated the key lithioaziridine intermediate, followed by cyclization and aromatization of the pyrrole ring t

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