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21987-25-7

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21987-25-7 Usage

General Description

5-methoxy-3-methyl-1H-indole is a chemical compound with the molecular formula C11H11NO. It belongs to the indole class of organic compounds and is characterized by a five-membered ring structure with a nitrogen atom. 5-methoxy-3-methyl-1H-indole is commonly found in the roots of some plant species and is known for its potential medicinal properties, including anti-inflammatory and anti-cancer effects. It has also been studied for its role in the synthesis of pharmaceutical compounds and is being researched for its potential applications in drug development. Overall, 5-methoxy-3-methyl-1H-indole is a versatile and biologically relevant compound with potential applications in various fields of science and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 21987-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,8 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21987-25:
(7*2)+(6*1)+(5*9)+(4*8)+(3*7)+(2*2)+(1*5)=127
127 % 10 = 7
So 21987-25-7 is a valid CAS Registry Number.

21987-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-3-methyl-1H-indole

1.2 Other means of identification

Product number -
Other names YSOFHURJVUIKMU-UHFFFAOYSA

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:21987-25-7 SDS

21987-25-7Relevant articles and documents

Ruthenium-catalysed synthesis of indoles from anilines and trialkanolamines in the presence of tin(II) chloride dihydrate

Cho, Chan Sik,Lim, Hyo Kyun,Shim, Sang Chul,Kim, Tae Jeong,Choi, Heung-Jin

, p. 995 - 996 (2007/10/03)

Anilines react with trialkanolamines in dioxane in the presence of a catalytic amount of a ruthenium catalyst together with tin(II) chloride dihydrate to give the corresponding indoles in moderate to good yields.

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