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807632-87-7

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807632-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 807632-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,7,6,3 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 807632-87:
(8*8)+(7*0)+(6*7)+(5*6)+(4*3)+(3*2)+(2*8)+(1*7)=177
177 % 10 = 7
So 807632-87-7 is a valid CAS Registry Number.

807632-87-7Downstream Products

807632-87-7Relevant academic research and scientific papers

A novel lipase enzyme panel exhibiting superior activity and selectivity over lipase B from Candida antarctica for the kinetic resolution of secondary alcohols

O'Neill, Maeve,Beecher, Denis,Mangan, David,Rowan, Andrew S.,Monte, Agnieszka,Sroka, Stefan,Modregger, Jan,Hundle, Bhupinder,Moody, Thomas S.

, p. 583 - 586 (2012)

A novel, commercially available lipase enzyme panel performing kinetic bioresolutions of a number of secondary alcohols is reported. The secondary alcohols that have been chosen are known from the literature to be particularly challenging substrates to resolve. Following initial screening, four co-solvents were investigated for each lead enzyme in an effort to assess their tolerance to common organic solvents. The superiority of these novel enzymes over lipase B from Candida antarctica (CALB) has been demonstrated.

Novel Intermediate of L-Cloperastine and Preparation Method Thereof

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Paragraph 0025-0029, (2016/12/01)

The present invention refers to pharmaceutically useful as well as novel intermediates of [...][...] -L (cloperastine) manufacturing method relates to and, more specifically a device with structure of formula 1 L- [...] intermediates manufacturing method of using enzymes relates to. Formula 1 , The, R the C1-C3 copyright 2000. (by machine translation)

Kinetic resolution of diarylmethanols using a mutated variant of lipase CALB

Engstr?m, Karin,Vallin, Michaela,Hult, Karl,B?ckvall, Jan-E.

, p. 7613 - 7618 (2012/09/07)

An enzymatic kinetic resolution of diarylmethanols via acylation has been developed. This was achieved by the use of a mutated variant of CALB that accepts larger substrates compared to the wild type. By the use of diarylmethanols with two differently sized aryl groups, enantioselective transformations were achieved. A larger size-difference led to a higher enantioselectivity. In addition, substrates with electronically different aryl groups, such as phenyl and pyridyl, also gave an enantioselective reaction. The highest E value was observed with a substrate where steric and electronic effects were combined.

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