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(S,E)-benzyl 2-methyl-2-(propionylthio)hex-3-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1067221-66-2

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1067221-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1067221-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,7,2,2 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1067221-66:
(9*1)+(8*0)+(7*6)+(6*7)+(5*2)+(4*2)+(3*1)+(2*6)+(1*6)=132
132 % 10 = 2
So 1067221-66-2 is a valid CAS Registry Number.

1067221-66-2Downstream Products

1067221-66-2Relevant academic research and scientific papers

Synthesis and biological activity of enantiomeric pairs of 5-(alk-2-enyl)thiolactomycin and 5-[(E)-cycloalk-2-enylidenemethyl] thiolactomycin congeners

Ohata, Kohei,Terashima, Shiro

experimental part, p. 920 - 936 (2010/03/23)

The title compounds were synthesized by the efficient route previously explored for the synthesis of enantiomeric pairs of thiolactomycin and its 3-demethyl derivative. These studies were carried out to prove the flexibility of the previously explored synthetic route to natural thiolactomycin (TLM) 1 and to examine the structure-activity relationship on the 5-position of 1. While all of the synthesized congeners lacked in vitro antibacterial activity, these studies led us to find 5-(alk-2-enyl)-TLM (ent-4d) which exhibits mammalian type I fatty acid synthase (FAS) inhibitory activity equal to that of C75, a potent inhibitor reported previously. It was also found that 5-[(E)-cycloalk-2- enylidenemethyl]-TLM (ent-5c) exhibited slightly less potent mammalian type I FAS inhibitory activity than C75.

Synthesis and biological activity of enantiomeric pairs of 5-vinylthiolactomycin congeners

Ohata, Kohei,Terashima, Shiro

, p. 4070 - 4074 (2008/02/07)

Twelve enantiomeric pairs of 5-vinylthiolactomycin congeners were synthesized by employing our efficient synthetic route previously explored for the synthesis of enantiomeric pairs of thiolactomycin and its 3-demethyl derivative. From the biological activ

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