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113566-74-8

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113566-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113566-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,6 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113566-74:
(8*1)+(7*1)+(6*3)+(5*5)+(4*6)+(3*6)+(2*7)+(1*4)=118
118 % 10 = 8
So 113566-74-8 is a valid CAS Registry Number.

113566-74-8Relevant articles and documents

PRODRUGS OF CHLOROKYNURENINES

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Paragraph 00121; 00124, (2017/03/28)

The present disclosure relates to prodrugs of 7-chlorokynurenic acid. In certain embodiments, the prodrugs include those having the structure of any one of formula (I)-(VIII), wherein R1-R13, monomer 1, monomer 2, and linker are defi

Enantioselective syn and anti homocrotylation of aldehydes: Application to the formal synthesis of spongidepsin

Lin, Hongkun,Tian, Leiming,Krauss, Isaac J.

supporting information, p. 13176 - 13182 (2015/10/28)

Whereas crotylboration has been a useful method for synthesis of stereochemically complex products, we have shown that homocrotylboration can be achieved with cyclopropanated crotylation reagents, and that the stereoselectivity of the reaction can be predicted by analogous models. This paper presents a full account of this work, including the first examples of asymmetric anti homocrotylation. The scope of this reaction is demonstrated with highly enantioselective homocrotylation of both aliphatic and aromatic aldehydes, as well as double diastereoselection studies. An application of the synthesis of the marine natural product spongidepsin is presented, as well as streamlined syntheses of homocrotylation reagents.

Kinetic resolution of 1,2-diols using nitrogen-tethered bisimidazoline-copper(I) catalyzed benzoylation

Arai, Takayoshi,Mizukami, Tomoe,Mishiro, Asami,Yanagisawa, Akira

experimental part, p. 995 - 1000 (2009/06/28)

Nitrogen-tethered bisimidazoline (Nb-imidazoline) ligand was utilized in the Cu(I)-catalyzed benzoylation of 1,2-diols. With the assistance of i-Pr2NEt, the reaction of rac-1,2-diols with o-methylbenzoyl chloride was smoothly catalyzed by Nb-imidazoline-CuCl in CH2Cl2 to give the corresponding o-methylbenzoylated secondary alcohols in up to 79% ee.

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