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(4-phenethyloxyphenyl)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

887360-10-3

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887360-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 887360-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,3,6 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 887360-10:
(8*8)+(7*8)+(6*7)+(5*3)+(4*6)+(3*0)+(2*1)+(1*0)=203
203 % 10 = 3
So 887360-10-3 is a valid CAS Registry Number.

887360-10-3Downstream Products

887360-10-3Relevant academic research and scientific papers

PIPERAZINE AND PIPERIDINE MGLUR5 POTENTIATORS

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Page/Page column 34, (2008/12/07)

Compounds of Formula I or pharmaceutically acceptable salts or solvates thereof, wherein A, B, D, Ar1, Ar2, R2, R3, R4, a, m and n are defined in the specification, methods for the use thereof, processes for making and pharmaceutical compositions containing the same.

Synthesis and aldose reductase inhibitory activities of novel O-substituted hydroxyphenylacetic acid derivatives

Rakowitz, Dietmar,Angerer, Helga,Matuszczak, Barbara

, p. 547 - 558 (2007/10/03)

In continuation of our work aimed towards the preparation of novel aldose reductase inhibitors, several O-substituted hydroxyphenylacetic acid derivatives were investigated. The highest inhibitory activity was found for compounds 7b and 7c bearing a cyclo

Novel, potent, selective, and orally bioavailable human βII-tryptase inhibitors

Sperandio, David,Tai, Vincent W.-F.,Lohman, Julia,Hirschbein, Bernie,Mendonca, Rohan,Lee, Chang-Sun,Spencer, Jeffrey R.,Janc, James,Nguyen, Margaret,Beltman, Jerlyn,Sprengeler, Paul,Scheerens, Heleen,Lin, Tong,Liu, Liang,Gadre, Ashwini,Kellogg, Alisha,Green, Michael J.,McGrath, Mary E.

, p. 4085 - 4089 (2007/10/03)

The synthesis of novel [1,2,4]oxadiazoles and their structure-activity relationship (SAR) for the inhibition of tryptase and related serine proteases is presented. Elaboration of the P′-side afforded potent, selective, and orally bioavailable tryptase inhibitors.

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