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4-(3,4-dimethoxythiophenoxy)butyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60169-55-3

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60169-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60169-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,6 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60169-55:
(7*6)+(6*0)+(5*1)+(4*6)+(3*9)+(2*5)+(1*5)=113
113 % 10 = 3
So 60169-55-3 is a valid CAS Registry Number.

60169-55-3Relevant academic research and scientific papers

Synthesis and platelet-activating factor (PAF)-antagonistic activities of 1,4-disubstituted piperazine derivatives

Fukushi,Mabuchi,Itoh,Terashita,Nishikawa,Sugihara

, p. 541 - 550 (2007/10/02)

During the screening of novel platelet-activating factor (PAF) antagonists, we found that 1-(6-methoxy-3,4-dihydro-2-naphthoyl)-4-(3,4,5- trimethoxybenzyl)piperazine and its 4-(3,4,5-trimethoxybenzoyl)piperazine derivatives (1b, 2b) exerted in vitro and i

PAF antagonist, 1,4-disubstituted piperazine compounds and production thereof

-

, (2008/06/13)

Platelet Activating Factor (PAF) antagonists which comprises the compounds of the formula (I): wherein A is an optionally substituted phenyl or an optionally substituted heterocyclic group; X is methylene group, carbonyl group or thiocarbonyl group; R1, R2 and R3 are independently a lower alkyl group, and their salts are excellent in absorption from the intestinal canal. Among the compounds of the formula (I), those wherein A is an optionally substituted 2,3-dihydro-1-benzoxepin-4--yl group are novel compounds and exhibit excellent PAF antagonism.

PAF antagonist, 1,4-disubstituted piperazine compounds and production thereof

-

, (2008/06/13)

Platelet Activating Factor (PAF) antagonists which comprise the compounds of the formula (I): STR1 wherein A is an optionally substituted phenyl or an optionally substituted heterocyclic group; X is methylene group, carbonyl group or thiocarbonyl group; R1, R2 and R3 are independently a lower alkyl group, and their salts are excellent in absorption from the intestinal canal. Among the compounds of the formula (I), those wherein A is an optionally substituted 2,3-dihydro-1-benzoxepin-4-yl group are novel compounds and exhibit excellent PAF antagonism.

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