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120417-13-2

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120417-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120417-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,1 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120417-13:
(8*1)+(7*2)+(6*0)+(5*4)+(4*1)+(3*7)+(2*1)+(1*3)=72
72 % 10 = 2
So 120417-13-2 is a valid CAS Registry Number.

120417-13-2Downstream Products

120417-13-2Relevant articles and documents

A library of spirooxindoles based on a stereoselective three-component coupling reaction

Lo, Michael M.-C.,Neumann, Christopher S.,Nagayama, Satoshi,Perlstein, Ethan O.,Schreiber, Stuart L.

, p. 16077 - 16086 (2004)

A collection of structurally complex and chemically diverse small molecules is a useful tool to explore cell circuitry. In this article, we report the split-pool synthesis of more than 3000 spirooxindoles on high capacity macrobeads. The key reaction to a

Direct Conversion of N-Alkylamines to N-Propargylamines through C-H Activation Promoted by Lewis Acid/Organocopper Catalysis: Application to Late-Stage Functionalization of Bioactive Molecules

Chan, Jessica Z.,Yesilcimen, Ahmet,Cao, Min,Zhang, Yuyang,Zhang, Bochao,Wasa, Masayuki

supporting information, p. 16493 - 16505 (2020/10/26)

An efficient catalytic method to convert an α-C-H bond of N-alkylamines into an α-C-alkynyl bond was developed. In the past, such transformations were carried out under oxidative conditions, and the enantioselective variants were confined to tetrahydroisoquinoline derivatives. Here, we disclose a method for the union of N-alkylamines and trimethylsilyl alkynes, without the presence of an external oxidant and promoted through cooperative actions of two Lewis acids, B(C6F5)3 and a Cu-based complex. A variety of propargylamines can be synthesized in high diastereo-and enantioselectivity. The utility of the approach is demonstrated by the late-stage site-selective modification of bioactive amines. Kinetic investigations that shed light on various mechanistic nuances of the catalytic process are presented.

FUSED TRIAZOLE AGONISTS OF THE APJ RECEPTOR

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Paragraph 0291-0292, (2019/05/22)

Compounds of Formula I, pharmaceutically acceptable salts thereof, tautomers thereof, pharmaceutically acceptable salts of the tautomers, or mixtures thereof are agonists of the APJ Receptor and may have use in treating cardiovascular and other conditions. Compounds of Formula (I) have the following structure: where the definitions of the variables are provided herein.

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