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2-chloro-N-(4-iodophenyl)-N-methylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

641612-92-2

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641612-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 641612-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,1,6,1 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 641612-92:
(8*6)+(7*4)+(6*1)+(5*6)+(4*1)+(3*2)+(2*9)+(1*2)=142
142 % 10 = 2
So 641612-92-2 is a valid CAS Registry Number.

641612-92-2Relevant academic research and scientific papers

Cellular localisation of structurally diverse diphenylacetylene fluorophores

Adams, Candace,Ambler, Carrie A.,Bain, Angus J.,Blacker, Thomas S.,Callaghan, Daniel,Chisholm, David R.,Girkin, John M.,Hughes, Joshua G.,Humann, Rachel,Lembicz, Nicola K.,Pujol, Alba,Whiting, Andrew

, p. 9231 - 9245 (2020)

Fluorescent probes are increasingly used as reporter molecules in a wide variety of biophysical experiments, but when designing new compounds it can often be difficult to anticipate the effect that changing chemical structure can have on cellular localisa

FLUORESCENT SYSTEMS FOR BIOLOGICAL IMAGING AND USES THEREOF

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Page/Page column 26; 28-29, (2021/02/12)

The invention relates to compounds of formula I, in which Y, Ar1, Ar2, X, R1 and R2 are defined herein, and to their use in a variety of biological imaging techniques and therapeutic methods. In aspects, the invention relates to conjugates comprising the compounds of formula I and their associated uses and therapeutic uses.

Sulfonylaminovalerolactams and derivatives thereof as factor Xa inhibitors

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Page/Page column 48, (2008/06/13)

The present application describes sulfonylaminovalerolactams and derivatives thereof of Formula I: or pharmaceutically acceptable salt forms thereof, wherein ring G is a mono- or bicyclic carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.

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