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4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193903-32-1

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193903-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193903-32-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,9,0 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193903-32:
(8*1)+(7*9)+(6*3)+(5*9)+(4*0)+(3*3)+(2*3)+(1*2)=151
151 % 10 = 1
So 193903-32-1 is a valid CAS Registry Number.

193903-32-1Relevant academic research and scientific papers

HETEROARYLDIHYDROPYRIMIDINE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS

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Page/Page column 36; 37, (2019/01/17)

Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.

IMMUNOREGULATORY AGENTS

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Paragraph 0355, (2016/01/27)

Compounds that modulate the oxidoreductase enzyme indoleamine 2,3-dioxygenase, and compositions containing the compounds, are described herein. The use of such compounds and compositions for the treatment and/or prevention of a diverse array of diseases, disorders and conditions, including cancer- and immune-related disorders, that are mediated by indoleamine 2,3-dioxygenase is also provided.

4-Amino substituted-2-substituted-1,2,3,4-tetrahydroquinoline compounds

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Page/Page column 44, (2010/10/20)

4-Amino substituted-2-substituted-1,2,3,4-tetrahydroquinoline compounds, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lowe

Fibrinogen receptor antagonists

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, (2008/06/13)

This invention relates to compounds of the formula: which are effective for inhibiting platelet aggregation, pharmaceutical compositions for effecting such activity, and a method for inhibiting platelet aggregation.

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