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5-CHLORO-3-METHYLINDOLE is a chlorinated derivative of 3-methylindole, a heterocyclic aromatic compound with the molecular formula C9H8ClN.
Used in Pharmaceutical Industry:
5-CHLORO-3-METHYLINDOLE is used as an intermediate in the synthesis of various drugs and pharmaceuticals for its potential role in creating new therapeutic agents.
Used in Biological Research:
5-CHLORO-3-METHYLINDOLE is used as a subject of study for its potential biological activities, including its effects on the central nervous system and as an antifungal agent, to explore its possible applications in medicine.
Used in Dye or Pigment Production:
5-CHLORO-3-METHYLINDOLE may have potential applications in the production of dyes or pigments due to its chemical structure, although more research is needed to fully understand its properties and potential uses in this industry.

71095-42-6

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71095-42-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71095-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,9 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71095-42:
(7*7)+(6*1)+(5*0)+(4*9)+(3*5)+(2*4)+(1*2)=116
116 % 10 = 6
So 71095-42-6 is a valid CAS Registry Number.

71095-42-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 5-chloro-3-methyl-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:71095-42-6 SDS

71095-42-6Relevant academic research and scientific papers

Active and Recyclable Catalytic Synthesis of Indoles by Reductive Cyclization of 2-(2-Nitroaryl)acetonitriles in the Presence of Co-Rh Heterobimetallic Nanoparticles with Atmospheric Hydrogen under Mild Conditions

Choi, Isaac,Chung, Hyunho,Park, Jang Won,Chung, Young Keun

, p. 5508 - 5511 (2016/11/17)

A cobalt-rhodium heterobimetallic nanoparticle-catalyzed reductive cyclization of 2-(2-nitroaryl)acetonitriles to indoles has been achieved. The tandem reaction proceeds without any additives under the mild conditions (1 atm H2 and 25 °C). This procedure could be scaled up to the gram scale. The catalytic system is significantly stable under these reaction conditions and could be reused more than ten times without loss of catalytic activity.

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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