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(S)-4-cyclohexyl-but-3-yn-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

853748-83-1

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853748-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853748-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,7,4 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 853748-83:
(8*8)+(7*5)+(6*3)+(5*7)+(4*4)+(3*8)+(2*8)+(1*3)=211
211 % 10 = 1
So 853748-83-1 is a valid CAS Registry Number.

853748-83-1Relevant articles and documents

Kinetic resolution of propargylic alcohols catalyzed by benzotetramisole

Birman, Vladimir B.,Guo, Lei

, p. 4859 - 4861 (2006)

(Chemical Equation Presented) Kinetic resolution of variously substituted secondary propargylic alcohols catalyzed by benzotetramisole (BTM) proceeds with selectivity factors up to 32, the highest ever achieved with nonenzymatic catalysts for this class o

Enantioselective and regioselective nickel-catalyzed multicomponent coupling of chiral allenes, aromatic aldehydes, and silanes

Ng, Sze-Sze,Jamison, Timothy F.

, p. 11405 - 11417 (2007/10/03)

A detailed account of the development of a recently developed, nickel-catalyzed multicomponent coupling of chiral allenes, aromatic aldehydes, and silanes is described. The axial chirality of the allene is transferred completely to the product, a trisubstituted Z-allylic alcohol protected as a silyl ether. A very high preference for sp rather than sp2 coupling is observed, and differentially substituted allenes undergo highly site-selective coupling. These transformations represent the first enantioselective multi-component coupling processes of allenes.

Highly enantioselective and regioselective nickel-catalyzed coupling of allenes, aldehydes, and silanes

Ng, Sze-Sze,Jamison, Timothy F.

, p. 7320 - 7321 (2007/10/03)

A complex derived from Ni(cod)2 and NHC-IPr catalyzes a three-component coupling reaction involving allenes, aldehydes, and organosilanes and transfers the axial chirality of the allene to a stereogenic center in the product with very high fide

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