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3-[4-[1-(2-cyano-5-methyl pyrrolyl)]benzyl]-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142015-75-6

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142015-75-6 Usage

General Description

The chemical compound 3-[4-[1-(2-cyano-5-methyl pyrrolyl)]benzyl]-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine, which has a molecular formula of C26H26N4, is a heterocyclic compound with potential pharmaceutical applications. It contains an imidazo[4,5-b]pyridine core structure and a benzyl group attached to a pyrrolyl moiety. 3-[4-[1-(2-cyano-5-methyl pyrrolyl)]benzyl]-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine may have potential biological activity due to its structural features, such as the cyano and methyl functional groups. However, specific properties and uses of this chemical are subject to further research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 142015-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,1 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 142015-75:
(8*1)+(7*4)+(6*2)+(5*0)+(4*1)+(3*5)+(2*7)+(1*5)=86
86 % 10 = 6
So 142015-75-6 is a valid CAS Registry Number.

142015-75-6Relevant academic research and scientific papers

Pilot scale synthesis of a novel nonpeptide angiotensin II receptor antagonist

Zanka, Atsuhiko,Nishiwaki, Masanori,Morinaga, Yasuhiro,Inoue, Takayuki

, p. 230 - 237 (2013/09/08)

FR143187 is a novel nonpeptide angiotensin II receptor antagonist under development at Fujisawa Pharmaceutical Co. for the treatment of hypertension. Development of a process for preparation on a large scale is described. The optimized process is 10 steps in length and uses only commercially available materials for each step. Efficient methylation of the 2-position of a pyrrole derivative was achieved by reduction of a Mannich base via the quaternary ammonium salt. Selective cyanation directed by a solvent effect was also investigated. Process improvement efforts focused on optimized reaction conditions for each step, leading to a high-quality product according to a new and concise synthetic route.

ANGIOTENSIN II ANTAGONIZING HETEROCYCLIC DERIVATIVES

-

, (2008/06/13)

The invention relates to compounds of the formula STR1 wherein STR2 represents a condensed or uncondensed imidazolyl ring and the rest of the variables are as defined in the specification. They are angiotensin II antagonists useful for treating hypertension, etc..

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