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N-[2-(4-aminophenyl)propyl]acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40377-40-0

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40377-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40377-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,7 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40377-40:
(7*4)+(6*0)+(5*3)+(4*7)+(3*7)+(2*4)+(1*0)=100
100 % 10 = 0
So 40377-40-0 is a valid CAS Registry Number.

40377-40-0Downstream Products

40377-40-0Relevant academic research and scientific papers

Quinazoline derivatives and its preparation method and application

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, (2019/07/08)

The invention relates to quinazoline derivatives and its preparation method and application. The quinazoline derivatives with The structural formula, the quinazoline derivative to gefitinib for the positive control, the result shows that compared with the gefitinib has good activity; and lead compound OTS514 compared, equivalent activity, PBK/TOPK inhibitors for further transformation and the discovery of new anti-tumor medicine phenological shopping has higher learning with the reference value. The invention also provides a preparation method of the quinazoline derivatives and the preparation of PBK/TOPK inhibitor and an anticancer drug.

NOVEL ACETYL-COA CARBOXYLASE (ACC) INHIBITORS AND THEIR USE IN DIABETES, OBESITY AND METABOLIC SYNDROME

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Page/Page column 23, (2008/06/13)

The present invention relates to compounds of formula (I) which inhibit acetyl-CoA carboxylase (ACC) and are useful for the prevention or treatment of metabolic syndrome, type II diabetes, obesity, atherosclerosis and cardiovascular diseases in humans.

Potential antiinflammatory compounds. I. Antiinflammatory phenylpiperidine derivatives

Hicks,Smith,Williamson,Day

, p. 1460 - 1464 (2007/10/05)

The syntheses of a number of amines and their derivatives, based on the phenylpiperidine nucleus, are described. Their activities on the rat paw carrageenan test are also reported. Activities comparable to that of phenylbutazone were obtained for some of

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