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1-(1-methyl-1H-indol-2-yl)ethanol is a chemical compound with the molecular formula C11H13NO, belonging to the indole class of heterocyclic aromatic compounds. This white to light brown solid is characterized by a strong odor and is recognized for its floral and woody scent.
[Data of usage]:
Used in Fragrance Industry:
1-(1-methyl-1H-indol-2-yl)ethanol is used as a fragrance ingredient for its floral and woody scent, adding depth and complexity to perfumes and other scented products.
Used in Pharmaceutical Synthesis:
1-(1-methyl-1H-indol-2-yl)ethanol is used as a key intermediate in the synthesis of various pharmaceuticals, leveraging its unique chemical structure to create novel medicinal compounds.
Used in Organic Chemistry:
1-(1-methyl-1H-indol-2-yl)ethanol is used as a building block in organic chemistry for the creation of diverse organic compounds, taking advantage of its reactive functional groups and structural features.
Used in Medical Applications:
1-(1-methyl-1H-indol-2-yl)ethanol has potential applications in the field of medicine, where its unique chemical properties may contribute to the development of new therapeutic agents or diagnostic tools.

29124-10-5

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29124-10-5 Usage

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 academic research and scientific papers

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.

Synthesis of highly substituted indene derivatives by Br?nsted acid catalyzed Friedel-Crafts reaction of homoallylic alcohols

Zhang, Xiaoxiang,Teo, Wan Teng,Rao, Weidong,Ma, Dik-Lung,Leung, Chung-Hang,Chan, Philip Wai Hong

supporting information, p. 3881 - 3884 (2014/07/08)

An efficient synthetic method to prepare highly substituted indenes in moderate to excellent yields that relies on Br?nsted acid catalyzed Friedel-Crafts reaction of homoallylic alcohols under mild conditions is described.

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

Indolecarbonyl Coupling Reactions Promoted by Samarium Diiodide. Application to the Synthesis of Indole-Fused Compounds

Lin, Shu-Chen,Yang, Fwu-Duo,Shiue, Jiann-Shyng,Yang, Shyh-Ming,Fang, Jim-Min

, p. 2909 - 2917 (2007/10/03)

By the assistance of an N-sulfonyl group or a cyano group at the C-2 position, hydroxyalkylations of indole-3-carbonyls were achieved by the promotion of samarium diiodide. The indolecarbonyl coupling reactions proceeded in high stereoselectivity via chel

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