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1,2,3-Trimethyl-1H-indole is an organic compound with the chemical formula C12H13N. It is a derivative of indole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to a pyrrole ring. The molecule has three methyl groups attached to the indole structure, with one methyl group at the 1st, 2nd, and 3rd positions. 1,2,3-Trimethyl-1H-indole is known for its strong, earthy odor and is used as a fragrance ingredient in various applications, such as perfumes and cosmetics. It is also found in nature, particularly in the essential oils of plants like jasmine and tuberose. Due to its complex structure and unique properties, 1,2,3-trimethyl-1H-indole has been a subject of interest in the fields of chemistry, biology, and materials science.

1971-46-6

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1971-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1971-46-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1971-46:
(6*1)+(5*9)+(4*7)+(3*1)+(2*4)+(1*6)=96
96 % 10 = 6
So 1971-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N/c1-8-9(2)12(3)11-7-5-4-6-10(8)11/h4-7H,1-3H3

1971-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-trimethylindole

1.2 Other means of identification

Product number -
Other names Indole,1,2,3-trimethyl

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:1971-46-6 SDS

1971-46-6Relevant academic research and scientific papers

Facile regiospecific synthesis of 2,3-disubstituted indoles from isatins

Dou, Xiaowei,Yao, Weijun,Wen, Shan,Lu, Yixin

supporting information, p. 9469 - 9472 (2014/08/18)

A facile regiospecific synthesis of 2,3-disubstituted indoles from isatins has been developed. Nucleophilic addition of Grignard reagents to commercially available isatins, followed by reduction with borane, afforded an array of structurally diverse 2,3-disubstituted indoles in moderate to good yields. The method described herein represents a novel and very simple approach to synthesize various 2,3-disubstituted indoles, extremely important structural motifs in the pharmaceutical industry and medicinal chemistry. This journal is the Partner Organisations 2014.

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