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29124-10-5

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29124-10-5 Usage

General Description

1-(1-methyl-1H-indol-2-yl)ethanol is a chemical compound with the molecular formula C11H13NO. It is a derivative of indole, a heterocyclic aromatic compound. This chemical is a white to light brown solid with a strong odor, which is used in the fragrance industry due to its floral and woody scent. It is also used in the synthesis of various pharmaceuticals and organic compounds. 1-(1-methyl-1H-indol-2-yl)ethanol has potential applications in the field of medicine and organic chemistry due to its unique chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 29124-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,2 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29124-10:
(7*2)+(6*9)+(5*1)+(4*2)+(3*4)+(2*1)+(1*0)=95
95 % 10 = 5
So 29124-10-5 is a valid CAS Registry Number.

29124-10-5SDS

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 1-(1-methylindol-2-yl)ethanol

1.2 Other means of identification

Product number -
Other names 1-(1-methyl-indol-2-yl)-ethanol

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:29124-10-5 SDS

29124-10-5Relevant articles and documents

One-Pot Assembly of 3-Hydroxycarbazoles via Uninterrupted Propargylation/Hydroxylative Benzannulation Reactions

Reddy, Chada Raji,Subbarao, Muppidi,Sathish, Puppala,Kolgave, Dattahari H.,Donthiri, Ramachandra Reddy

supporting information, p. 689 - 693 (2020/01/31)

A novel strategy for the synthesis of 3-hydroxycarbazoles involving the consecutive propargylation/palladium-catalyzed hydroxylative benzannulation of indole-2-carbonyls with propargylic alcohols has been exploited. This one-pot procedure leads to a wide range of substituted 3-hydroxycarbazoles in high yield with a broad substrate scope. The method was further extended to access furano-carbazole derivatives from dialkynols via tandem annulations.

Di- and triheteroarylalkanes via self-condensation and intramolecular Friedel-Crafts type reaction of heteroaryl alcohols

Dhiman, Seema,Ramasastry

supporting information, p. 8030 - 8035 (2013/12/04)

An efficient synthetic approach to diheteroarylmethanes and 1,3-diheteroarylpropenes has been developed via Yb(iii)-catalyzed sequential self-condensation of 2-furfuryl (or 2-thienyl or 3-indolyl) alcohols followed by intramolecular Friedel-Crafts type re

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