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3-Pyridinemethanol,6-ethenyl-(9CI) is a chemical compound with the molecular formula C8H9NO. It is a derivative of pyridine and contains an ethenyl group, also known as a vinyl group, attached to the sixth carbon atom of the pyridine ring. 3-Pyridinemethanol,6-ethenyl-(9CI) is known for its potential biological activity and is often used in organic synthesis and as a building block for the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It may also be used as a reagent in various chemical reactions due to its unique structure and properties.

432554-92-2

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432554-92-2 Usage

Uses

Used in Pharmaceutical Industry:
3-Pyridinemethanol,6-ethenyl-(9CI) is used as a building block for the production of pharmaceuticals for its potential biological activity and unique structure.
Used in Agrochemical Industry:
3-Pyridinemethanol,6-ethenyl-(9CI) is used as a building block for the production of agrochemicals due to its potential applications in the development of new drugs or treatment methods.
Used in Specialty Chemicals Industry:
3-Pyridinemethanol,6-ethenyl-(9CI) is used as a building block for the production of specialty chemicals for its unique structure and properties.
Used in Organic Synthesis:
3-Pyridinemethanol,6-ethenyl-(9CI) is used as a reagent in various chemical reactions for its potential applications in the development of new drugs or treatment methods.

Check Digit Verification of cas no

The CAS Registry Mumber 432554-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,2,5,5 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 432554-92:
(8*4)+(7*3)+(6*2)+(5*5)+(4*5)+(3*4)+(2*9)+(1*2)=142
142 % 10 = 2
So 432554-92-2 is a valid CAS Registry Number.

432554-92-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-ethenylpyridin-3-yl)methanol

1.2 Other means of identification

Product number -
Other names G-5060

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:432554-92-2 SDS

432554-92-2Downstream Products

432554-92-2Relevant academic research and scientific papers

Isoxazolines as Therapeutic Agents

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Paragraph 0702-0703, (2013/03/26)

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

Optimization of 5-vinylaryl-3-pyridinecarbonitriles as PKCθ inhibitors

Boschelli, Diane H.,Subrath, Joan,Niu, Chuansheng,Wu, Biqi,Wang, Yan,Lee, Julie,Brennan, Agnes,Ho, Melisa,Deng, Bijia,Yang, Xiaoke,Xu, Xin,Leung, Louis,Wang, Jianyao,Atherton, James,Chaudhary, Divya

scheme or table, p. 1965 - 1968 (2010/06/20)

Analog 8, a 3-pyridinecarbonitrile with an (E)-2-{6-[(4-methylpiperazin-1-yl)methyl]pyridin-2-yl}vinyl group at C-5, had an IC50 value of 1.1 nM for the inhibition of PKCθ and potently blocked the production of IL-2 in both stimulated murine T cells (IC50 = 34 nM) and human whole blood (IC50 = 500 nM).

Optimization of 7-alkene-3-quinolinecarbonitriles as Src kinase inhibitors

Boschelli, Diane H.,Wang, Daniel,Wang, Yan,Wu, Biqi,Honores, Erick E.,Barrios Sosa, Ana Carolina,Chaudhary, Inder,Golas, Jennifer,Lucas, Judy,Boschelli, Frank

scheme or table, p. 2924 - 2927 (2010/07/04)

The 7-alkene-3-quinolinecarbonitrile 20, a potent inhibitor of Src enzymatic and cellular activity with IC50 values of 2.1 and 58 nM, respectively, had comparable efficacy to bosutinib in a colon tumor xenograft study.

5-ALKYL/ALKENYL-3-CYANOPYRIDINES AS KINASE INHIBITORS

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Page/Page column 170, (2009/07/17)

Described herein are compounds of formula I: wherein G is and pharmaceutically acceptable salts thereof, wherein J, X, R1, R2, R11, R12' and p are as defined herein. Also provided herein are methods of making the compounds of formula I, and methods of using these compounds for inhibiting or treating a pathological condition or disorder linked to or mediated by a protein kinase in a mammal.

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