56341-40-3 Usage
General Description
7-Trifluoromethyloxindole is a chemical compound that belongs to the oxindole family. It is an organic compound with the molecular formula C9H6F3NO and a molecular weight of 203.14 g/mol. 7-TRIFLUOROMETHYLOXINDOLE features a trifluoromethyl group and an oxindole substructure. It is commonly used in chemical and pharmaceutical research as a building block and intermediate in the synthesis of various biologically active molecules. The trifluoromethyl group contributes to the compound's unique reactivity and properties, making it valuable in the development of new drugs and materials. 7-Trifluoromethyloxindole has potential applications in medicinal chemistry and drug discovery, particularly in the design of novel pharmaceuticals with improved biological activity and pharmacokinetic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 56341-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,4 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56341-40:
(7*5)+(6*6)+(5*3)+(4*4)+(3*1)+(2*4)+(1*0)=113
113 % 10 = 3
So 56341-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F3NO/c10-9(11,12)6-3-1-2-5-4-7(14)13-8(5)6/h1-3H,4H2,(H,13,14)
56341-40-3Relevant articles and documents
A novel methodology for the efficient synthesis of 3-monohalooxindoles by acidolysis of 3-phosphate-substituted oxindoles with haloid acids
Liu, Li,Li, Yue,Huang, Tiao,Kong, Dulin,Wu, Mingshu
, p. 2321 - 2328 (2021/09/22)
A novel method for the synthesis of 3-monohalooxindoles by acidolysis of isatin-derived 3-phosphate-substituted oxindoles with haloid acids was developed. This synthetic strategy involved the preparation of 3-phosphate-substituted oxindole intermediates and SN1 reactions with haloid acids. This new procedure features mild reaction conditions, simple operation, good yield, readily available and inexpensive starting materials, and gram-scalability.
Selective reduction of carbonyl groups in the presence of low-valent titanium reagents
Lin, Wei,Hu, Ming-Hua,Feng, Xian,Fu, Lei,Cao, Cheng-Pao,Huang, Zhi-Bin,Shi, Da-Qing
, p. 2238 - 2242 (2014/04/17)
The chemoselective reduction of several structurally diverse compounds containing carbonyl groups was achieved in the presence of low-valent titanium reagents. This novel synthetic method provides easy access to highly selective reduction of carbonyl groups, and possesses several advantages including one-step procedure, convenient manipulation, good to excellent yields, and short reaction times.
