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Methanone, (2-amino-5-chlorophenyl)(2-methyl-4-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

698395-59-4

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698395-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 698395-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,8,3,9 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 698395-59:
(8*6)+(7*9)+(6*8)+(5*3)+(4*9)+(3*5)+(2*5)+(1*9)=244
244 % 10 = 4
So 698395-59-4 is a valid CAS Registry Number.

698395-59-4Downstream Products

698395-59-4Relevant academic research and scientific papers

NEW ARYL-QUINOLINE DERIVATIVES

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, (2013/05/22)

The invention provides novel compounds having the general formula (I), wherein R1, R2, R3, R4 R5, R6 and n are as described herein, compositions including the compounds and methods of using the compounds.

ARYL-QUINOLINE DERIVATIVES

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, (2013/05/21)

The invention provides novel compounds having the general formula (I) wherein R1, R2, R3, R4, R5, R6 and n are as described herein, compositions including the compounds and methods of using the compounds. The present compounds are useful as fatty-acid binding protein (FABP) 4 and/or 5 inhibitors and may be used for the treatment or prophylaxis of lipodystrophy, type 2 diabetes, dyslipidemia, atherosclerosis, liver diseases involving inflammation, steatosis and/or fibrosis, such as non-alcoholic fatty liver disease, in particular non-alcoholic steatohepatitis, metabolic syndrome, obesity, chronic inflammatory and autoimmune inflammatory diseases.

ARYL SULFONAMIDES

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Page 55-56, (2008/06/13)

Compounds are provided that act as potent antagonists of the CCR9 receptor, and which have been further confirmed in animal testing for inflammation, one of the hallmark disease states for CCR9. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR9-mediated diseases, and as controls in assays for the identification of CCR9 antagonists.

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