415918-12-6 Usage
Uses
Used in Pharmaceutical Research:
1H-INDOLE-3-CARBOXYLIC ACID,6-(TRIFLUOROMETHYL)-,METHYL ESTER is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its unique structure and functional groups enable the design and synthesis of potential drug candidates with novel therapeutic properties.
Used in Agrochemical Development:
In the agrochemical industry, 1H-INDOLE-3-CARBOXYLIC ACID,6-(TRIFLUOROMETHYL)-,METHYL ESTER is employed as a precursor in the synthesis of new agrochemicals. Its chemical properties allow for the creation of compounds with potential applications in crop protection, pest control, and other agricultural areas.
Used in Material Science:
1H-INDOLE-3-CARBOXYLIC ACID,6-(TRIFLUOROMETHYL)-,METHYL ESTER is utilized as a building block in the development of new materials with specific properties. Its incorporation into various material systems can lead to the creation of innovative products with applications in different industries, such as electronics, coatings, and plastics.
Check Digit Verification of cas no
The CAS Registry Mumber 415918-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,5,9,1 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 415918-12:
(8*4)+(7*1)+(6*5)+(5*9)+(4*1)+(3*8)+(2*1)+(1*2)=146
146 % 10 = 6
So 415918-12-6 is a valid CAS Registry Number.
415918-12-6Relevant articles and documents
Palladium-catalyzed oxidative coupling of aromatic primary amines and alkenes under molecular oxygen: Stereoselective assembly of (Z)-enamines
Ji, Xiaochen,Huang, Huawen,Wu, Wanqing,Li, Xianwei,Jiang, Huanfeng
, p. 11155 - 11162 (2013/12/04)
An efficient Pd-catalyzed oxidative coupling of aromatic primary amines and alkenes under molecular oxygen is disclosed. Under mild reaction conditions, it provides a rapid access to (Z)-enamine compounds with exceptional functional group tolerance and ex
Solid-phase synthesis of indolecarboxylates using palladium-catalyzed reactions
Yamazaki, Kazuo,Nakamura, Yosuke,Kondo, Yoshinori
, p. 6011 - 6019 (2007/10/03)
Polymer-supported, palladium-catalyzed cyclization reactions effectively synthesized indolecarboxylates. Palladium-catalyzed carbon - carbon bond-forming reactions of immobilized enaminoesters followed by transesterification yielded indole 2- or 3-carboxylates with various functional groups on the benzene ring. Indolecarboxylates were efficiently cyclized via an intramolecular palladium-catalyzed amination reaction of immobilized N-substituted dehydrohalophenylalanines, and immobilized N-acetyl-dehydroalanines were efficiently converted into indolecarboxylates via tandem Heck-amination reactions.
