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(4-Amino-phenyl)-pyridin-3-yl-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147696-69-3

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147696-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147696-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,6,9 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 147696-69:
(8*1)+(7*4)+(6*7)+(5*6)+(4*9)+(3*6)+(2*6)+(1*9)=183
183 % 10 = 3
So 147696-69-3 is a valid CAS Registry Number.

147696-69-3Downstream Products

147696-69-3Relevant academic research and scientific papers

Urea thiadiazole inhibitors of plasminogen activator inhibior-1

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Page/Page column 21, (2010/02/11)

Methods of treating disorders associated with elevated levels of PAI-1 are disclosed comprising administering to a patient in need thereof a therapeutically effective amount of at least one compound of formula (I), or a pharmaceutically-acceptable salt, prodrug, stereoisomer or solvate thereof, wherein: A is aryl o heteroaryl, and R1-R12, are defined herein. The invention also pertains to pharmaceutical compositions and compounds within the scope of formula (I) as well as medicaments and articles of manufacture comprising compounds of formula (I).

Approach to dual-acting platelet activating factor (PAF) receptor antagonist/thromboxane synthase inhibitor (TxSI) based on the link of PAF antagonists and TxSIs

Fujita, Masakazu,Seki, Taketsugu,Inada, Haruaki,Shimizu, Kazuhiro,Takahama, Akane,Sano, Tetsuro

, p. 341 - 344 (2007/10/03)

A series of compounds (22-36) which possess dual-acting PAF antagonist/TxSI have been generated by the approach of linking the known PAF antagonists and TxIs, such as Ridogrel (1).

6,6-Disubstituted hex-5-enoic acid derivatives as combined thromboxane A2 receptor antagonists and synthetase inhibitors

Soyka,Heckel,Nickl,Eisert,Muller,Weisenberger

, p. 26 - 39 (2007/10/02)

A series of ω-disubstituted alkenoic acid derivatives were designed and synthesized as antithrombotic inhibitors of thromboxane A2 synthetase and thromboxane A2 receptor antagonists. Hexenoic acid derivatives with a 3- pyridyl group

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