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3,5-dimethyl-1H-indole is an organic compound with the molecular formula C10H11N. It is a derivative of the indole class, characterized by a fused pyrrole and benzene ring structure. The compound features two methyl groups attached to the indole nucleus, specifically at the 3rd and 5th positions. This chemical is known for its distinct odor and is often used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its unique properties, 3,5-dimethyl-1H-indole has potential applications in the development of new drugs and materials.

3189-12-6

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3189-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3189-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3189-12:
(6*3)+(5*1)+(4*8)+(3*9)+(2*1)+(1*2)=86
86 % 10 = 6
So 3189-12-6 is a valid CAS Registry Number.

3189-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-1H-indole

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl-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:3189-12-6 SDS

3189-12-6Relevant academic research and scientific papers

One-pot N-alkylation/Heck approach to substituted indoles

Weinrich, Melissa L.,Beck, Hilary P.

scheme or table, p. 6968 - 6972 (2010/02/27)

Here, we report the palladium-catalyzed one-pot N-alkylation/Heck cyclization of anilines to substituted indoles employing Pd(OAc)2/XPhos. The scope and limitations of this methodology will be described.

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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