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741290-77-7

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741290-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 741290-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,2,9 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 741290-77:
(8*7)+(7*4)+(6*1)+(5*2)+(4*9)+(3*0)+(2*7)+(1*7)=157
157 % 10 = 7
So 741290-77-7 is a valid CAS Registry Number.

741290-77-7Relevant articles and documents

SUBSTITUTED PYRROLIDINE COMPOUND AND USE THEREOF

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Paragraph 0665, (2020/12/25)

The present invention provides a substituted pyrrolidine compound having an orexin type 2 receptor agonist activity. A compound represented by the formula (I): wherein each symbol is as described in the specification, or a salt thereof, has an orexin type 2 receptor agonist activity, and is useful as an agent for the prophylaxis or treatment of narcolepsy.

Pyrimidine derivative, preparation method therefor and application thereof in medicine

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Paragraph 0250; 0251; 0252; 0253; 0254; 0255; 0256, (2016/10/07)

The invention relates to a pyrimidine derivative, a preparation method therefor and an application thereof in medicine. Particularly, the invention relates to a compound as shown in general formula (M) or a stereisomer, an aquo-complex, a metabolic product, a solvate, a pharmaceutically acceptable salt, a co-crystallization or a prodrug thereof; the preparation method thereof; and the application of the medicine composition thereof and the compound medicine compound in the medicine, particularly the application as an EGFR target spot inhibitor, wherein the definition of each substituent group in the general formula (M) is the same as that of the specification.

New orally active PDE4 inhibitors with therapeutic potential

Ochiai, Hiroshi,Ishida, Akiharu,Ohtani, Tazumi,Kusumi, Kensuke,Kishikawa, Katuya,Yamamoto, Susumu,Takeda, Hiroshi,Obata, Takaaki,Nakai, Hisao,Toda, Masaaki

, p. 4089 - 4100 (2007/10/03)

The design, synthesis, and biological evaluation of a series of pyrazolopyridines was carried out. Structural optimization of the aniline moiety of 4-anilinopyrazolopyridine derivative 3a, which is one of the newly discovered chemical leads for PDE4 inhib

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