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1248345-37-0

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1248345-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1248345-37-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,8,3,4 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1248345-37:
(9*1)+(8*2)+(7*4)+(6*8)+(5*3)+(4*4)+(3*5)+(2*3)+(1*7)=160
160 % 10 = 0
So 1248345-37-0 is a valid CAS Registry Number.

1248345-37-0Downstream Products

1248345-37-0Relevant articles and documents

Design, synthesis and anti-ulcerogenic effect of some of furo-salicylic acid derivatives on acetic acid-induced ulcerative colitis

Hassan, Ghaneya S.,Soliman, Gamal A.

, p. 4104 - 4112 (2010)

Ulcerative colitis is a chronically recurrent inflammatory bowel disease of unknown origin. The present work describes design and synthesis of 3-aminofurosalicylic acid 4, azo-conjugates with aniline 2a, 4-ASA 2b or sulphapyridine 2c as well as N-arylsulphonamido 5, chlorosulphonyl 6, aminosulphonyl 7 and N-arylaminosulphonyl derivatives 8 (positional isosters of 5). All the synthesized compounds were evaluated for their anti-ulcerogenic effect on acetic acid-induced ulcerative colitis in rats. It was noticed that oral treatment with sulphasalazine (a reference drug) and the tested compounds 2a, 2c, 4 and 5c in equimolar doses significantly reduced the intensity of lesion score, ulcer area, ulcer index and wet weight/length ratio compared to the control group. On the other hand, compounds 2b, 5a, 5b and 7 had a lower anti-ulcerogenic efficacy. Also, the antimicrobial activity of the synthesized compounds was screened in vitro using the agar diffusion assay technique. In addition, docking of the tested compounds into cycloxygenase II using molecular operating environment (MOE) was performed in order to rationalize the obtained biological results and their mechanism of action. The present work describes design and synthesis of 3-aminofurosalicylic acid 4, azo-conjugates 2a-c, N-arylsulphonamido 5, chlorosulphonyl 6, aminosulphonyl 7 and N-arylaminosulphonyl derivatives 8. All the synthesized compounds and sulphasalazine (a reference) were evaluated for their anti-ulcerogenic effect on acetic acid-induced ulcerative colitis in rats.

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