29124-10-5 Usage
Description
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.
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.
29124-10-5Relevant 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
