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Silane, tris(1-methylethyl)[(2S)-oxiranylmethoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

185140-87-8

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185140-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185140-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,1,4 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 185140-87:
(8*1)+(7*8)+(6*5)+(5*1)+(4*4)+(3*0)+(2*8)+(1*7)=138
138 % 10 = 8
So 185140-87-8 is a valid CAS Registry Number.

185140-87-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S)-oxiran-2-yl]methoxy-tri(propan-2-yl)silane

1.2 Other means of identification

Product number -
Other names (S)-3-Triisopropylsilyloxy-1,2-epoxypropane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:185140-87-8 SDS

185140-87-8Relevant academic research and scientific papers

MOENOMYCIN ANALOGS, METHODS OF SYNTHESIS, AND USES THEREOF

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Page/Page column 135-136, (2009/05/30)

The present invention provides novel moenomycin analogs as well as pharmaceutical compositions thereof, methods of synthesis, and methods of use in treating an infection by administering an inventive compound to a subject in need thereof. The moenomycin a

Degradation and reconstruction of moenomycin A and derivatives: Dissecting the function of the isoprenoid chain

Adachi, Masaatsu,Zhang, Yi,Leimkuhler, Catherine,Sun, Binyuan,LaTour, John V.,Kahne, Daniel E.

, p. 14012 - 14013 (2007/10/03)

Moenomycin A is the only known natural product that inhibits peptidoglycan biosynthesis by binding the bacterial transglycosylases. We describe a degradation/reconstruction route to manipulate the reducing end of moenomycin A. A comparison of the biological and enzyme inhibitory activity of moenomycin A and an analogue containing a nerol lipid in place of the natural C25 lipid chain provides insight into the role of the moenocinol unit. Our results show that a lipid chain having ten carbons in moenocinol is sufficient for enzyme inhibition, but a longer chain is required for biological acitivity, apparently because the molecule must partition into biological membranes to reach its target in bacterial cells. Copyright

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