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Cyclopropanecarboxaldehyde, 2-benzoyl-3-propyl-, (1R,2S,3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849582-79-2

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849582-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849582-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,5,8 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 849582-79:
(8*8)+(7*4)+(6*9)+(5*5)+(4*8)+(3*2)+(2*7)+(1*9)=232
232 % 10 = 2
So 849582-79-2 is a valid CAS Registry Number.

849582-79-2Downstream Products

849582-79-2Relevant academic research and scientific papers

Organocatalytic asymmetric cyclopropanation of α,β-unsaturated aldehydes with arsonium ylides

Zhao, Yun-Hui,Zhao, Gang,Cao, Wei-Guo

, p. 2462 - 2467 (2007)

A novel organocatalytic asymmetric cyclopropanation of α,β-unsaturated aldehydes with arsonium ylides using diphenylprolinol silylether as a catalyst is described. A variety of chiral cyclopropyl aldehydes are obtained in moderate to good yields with up t

Enantioselective organocatalytic cyclopropanations. The identification of a new class of iminium catalyst based upon directed electrostatic activation

Kunz, Roxanne K.,MacMillan, David W. C.

, p. 3240 - 3241 (2005)

A new method for enantioselective organocatalytic cyclopropanation is described. This study outlines the identification of a new class of iminium catalyst based on the concept of directed electrostatic activation (DEA). This novel organocatalytic mechanism exploits dual activation of ylide and enal substrates through a proposed electrostatic activation and stereodirected protocol. Formation of trisubstituted cyclopropanes with high levels of enantio- and diastereoinduction is accomplished for a variety of α,β-unsaturated aldehydes and sulfonium ylides. In addition, mechanistic studies have found that this cyclopropanation reaction exhibits enantioselectivity and reactivity profiles that are in accord with the proposed DEA step. Copyright

Tetrazolic acid functionalized dihydroindol: Rational design of a highly selective cyclopropanation organocatalyst

Hartikka, Antti,Arvidsson, Per I.

, p. 5874 - 5877 (2008/02/09)

(Chemical Equation Presented) Herein we wish to report our development of an improved catalyst (S)-(-)-indoline-2-yl-1H-tetrazole (1) for the enantioselective organocatalyzed cyclopropanation of α,β-unsaturated aldehydes with sulfur ylides. The new organo

Application of novel sulfonamides in enantioselective organocatalyzed cyclopropanation

Hartikka, Antti,Slosarczyk, Adam T.,Arvidsson, Per I.

, p. 1403 - 1409 (2008/02/10)

Three novel aryl sulfonamides derived from (2S)-indoline-2-carboxylic acid have been obtained and used as organocatalysts. The catalysts incorporate diverse functionality on the phenyl ring, enabling steric, and electronic fine tuning of the catalysts. Th

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