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131952-81-3

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131952-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131952-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,9,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131952-81:
(8*1)+(7*3)+(6*1)+(5*9)+(4*5)+(3*2)+(2*8)+(1*1)=123
123 % 10 = 3
So 131952-81-3 is a valid CAS Registry Number.

131952-81-3Relevant articles and documents

Identification of a novel fluoropyrrole derivative as a potassium-competitive acid blocker with long duration of action

Nishida, Haruyuki,Arikawa, Yasuyoshi,Hirase, Keizo,Imaeda, Toshihiro,Inatomi, Nobuhiro,Hori, Yasunobu,Matsukawa, Jun,Fujioka, Yasushi,Hamada, Teruki,Iida, Motoo,Nishitani, Mitsuyoshi,Imanishi, Akio,Fukui, Hideo,Itoh, Fumio,Kajino, Masahiro

supporting information, p. 3298 - 3314 (2017/05/29)

With the aim to find a novel long-lasting potassium-competitive acid blocker (P-CAB) that would perfectly overcome the limitations of proton pump inhibitors (PPIs), we tried various approaches based on pyrrole derivative 1b as a lead compound. As part of

4-fluorobenzoic compounds with 5-HT2 - and α1 -antagonistic activities

-

, (2008/06/13)

The invention relates to the compounds of general formula I: STR1 in which: m represents an integer from 2 to 4, n and p, which may be identical or different, each represent an integer from 1 to 3, q represents 0 or 1, and R represents: either a group of formula (A): STR2 or a radical of formula (B): STR3 or a 2,4-dioxo-1,2,3,4-tetrahydroquinazolinyl radical, on condition, however, that, in this case, n and p do not simultaneously represent the number 2, or a benzhydryloxy group, or a 1-oxophthalazinyl radical, or a 5-oxothiazolo[3,2-A]pyrimidinyl radical, or a group of formula C: STR4 their possible stereoisomers and their addition salts with a pharmaceutically acceptable inorganic or organic acid. The compounds of formula I are medicinal products with useful 5-HT2 - and α1 -antagonistic activities.

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