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

844864-99-9

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844864-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 844864-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,8,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 844864-99:
(8*8)+(7*4)+(6*4)+(5*8)+(4*6)+(3*4)+(2*9)+(1*9)=219
219 % 10 = 9
So 844864-99-9 is a valid CAS Registry Number.

844864-99-9Downstream Products

844864-99-9Relevant academic research and scientific papers

Synthesis of stereohomogeneous cyclopropanecarbaldehydes and cyclopropyl ketones by cycloalkylation of 4-hydroxy-1-alkenyl carbamates

Kalkofen, Rainer,Brandau, Sven,Wibbeling, Birgit,Hoppe, Dieter

, p. 6667 - 6669 (2004)

Small rings: Only a few methods are known for the synthesis of cyclopropane carbaldehydes and cyclopropyl ketones 2. In a new, simple route to highly enantioenriched trisubstituted three-membered rings, 4-hydroxy-1-alkenyl N,N-di-isopropyl carbamates 1 are treated with NaH, resulting in migration of the carbamoyl group and intramolecular enolate alkylation.

Enantio- and diastereoselective synthesis of highly substituted acylcyclopropanes from homoaldol products by stereospecific homoallylic cyclization

Kalkofen, Rainer,Brandau, Sven,Uenaldi, Seda,Frohlich, Roland,Hoppe, Dieter

, p. 4571 - 4580 (2007/10/03)

Highly enantioenriched 4-hydroxy-1-alkenyl N,N-diisopropylcarbamates, easily available by asymmetric homoaldol reaction, cyclize by treatment with sodium hydride to form (1r,2t,3t)-configured 1-acylcyclopropanes with high diastereoselectivity. The decisiv

Enantioselective synthesis of cyclopropanes by aldehyde homologation

Risatti, Christina A.,Taylor, Richard E.

, p. 6671 - 6672 (2007/10/03)

An efficient method for the enantioselective preparation of structurally diverse cyclopropanes has been developed. Sequential homoaldol coupling and activation steps result in a three-carbon homologation of an aldehyde to give a nonracemic, stereochemical

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