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4-aMino-3-Methyl-5-nitro-benzonitrile is an organic compound that serves as an intermediate in the synthesis of novel benzimidazoles. It plays a crucial role in the development of pharmaceuticals targeting specific receptors.
Used in Pharmaceutical Industry:
4-aMino-3-Methyl-5-nitro-benzonitrile is used as a chemical intermediate for the synthesis of benzimidazoles that act as inhibitors of insulin-like growth factor receptor-1 (IGF-1R). These benzimidazoles have potential applications in the treatment of various diseases and conditions by targeting and modulating the activity of IGF-1R.

468741-02-8

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468741-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 468741-02-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,8,7,4 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 468741-02:
(8*4)+(7*6)+(6*8)+(5*7)+(4*4)+(3*1)+(2*0)+(1*2)=178
178 % 10 = 8
So 468741-02-8 is a valid CAS Registry Number.

468741-02-8Relevant articles and documents

ROR NUCLEAR RECEPTOR MODULATORS

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Page/Page column 58, (2016/12/26)

The invention provides compounds of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treating immunological conditions.

NOVEL BENZIMIDAZOLE COMPOUND, PREPARATION METHOD THEREOF AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Page/Page column 84-85, (2011/09/15)

The present invention relates to a novel benzimidazole compound, a pharmaceutical composition for preventing or treating an inflammatory disease comprising said compound, a use of a novel benzimidazole compound for the manufacture of a medicament for prev

Imidazole moiety replacements in the 3-(1H-benzo[d]imidazol-2-yl)pyridin-2(1H)-one inhibitors of insulin-like growth factor receptor-1 (IGF-1R) to improve cytochrome P450 profile

Velaparthi, Upender,Liu, Peiying,Balasubramanian, Balu,Carboni, Joan,Attar, Ricardo,Gottardis, Marco,Li, Aixin,Greer, Ann,Zoeckler, Mary,Wittman, Mark D.,Vyas, Dolatrai

, p. 3072 - 3076 (2008/02/07)

A series of 3-(1H-benzo[d]imidazol-2-yl)pyridin-2(1H)-one inhibitors of insulin-like growth factor receptor-1 (IGF-1R) were examined in which the pendant imidazole moiety was replaced to improve selectivity for IGF-1R inhibition over cytochrome P450 (CYP). Synthesis and SAR of these compounds is presented.

Benzimidazole C-2 heterocycles as kinase inhibitors

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Page/Page column 15, (2010/02/11)

Benzimidazole derivatives having the general formula I are provided. These compounds are useful as tyrosine kinase inhibitors, especially for the treatment of cancer.

Novel tyrosine kinase inhibitors

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Page 27, (2010/11/30)

The present invention provides compounds of formula I and pharmaceutically acceptable salts thereof. The formula I compounds inhibit tyrosine kinase enzymes thereby making them useful as anti-cancer agents. The formula I compounds are also useful for the treatment of other diseases which can be treated by inhibiting tyrosine kinase enzymes.

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