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187392-96-7

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187392-96-7 Usage

Description

(5-phenylpyridin-3-yl)methanol, a chemical compound with the molecular formula C12H11NO, is a white to off-white crystalline powder that exhibits solubility in various organic solvents. It serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Known for its potential biological activity, this compound features anti-inflammatory and antioxidant properties, and has been investigated for its therapeutic potential in treating a range of diseases and conditions, establishing its significance in medicinal chemistry.

Uses

Used in Pharmaceutical Synthesis:
(5-phenylpyridin-3-yl)methanol is utilized as a key intermediate in the production of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for the creation of a variety of medicinal compounds with diverse applications.
Used in Agrochemical Production:
In the agrochemical industry, (5-phenylpyridin-3-yl)methanol is employed as a building block for the synthesis of various agrochemicals, including pesticides and herbicides, to enhance crop protection and yield.
Used in Medicinal Chemistry Research:
(5-phenylpyridin-3-yl)methanol is used as a research compound for exploring its potential biological activities, such as anti-inflammatory and antioxidant effects. Its study aids in understanding its role in the treatment of various diseases and conditions, advancing the discovery of novel therapeutic agents.
Used in Drug Development:
Owing to its potential use in the treatment of diseases, (5-phenylpyridin-3-yl)methanol is applied in drug development programs. It serves as a starting material for designing and synthesizing new pharmaceuticals with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 187392-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,3,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 187392-96:
(8*1)+(7*8)+(6*7)+(5*3)+(4*9)+(3*2)+(2*9)+(1*6)=187
187 % 10 = 7
So 187392-96-7 is a valid CAS Registry Number.

187392-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-phenylpyridin-3-yl)methanol

1.2 Other means of identification

Product number -
Other names 5-phenyl-3-pyridylmethanol

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:187392-96-7 SDS

187392-96-7Relevant articles and documents

IMIDAZOTHIADIAZOLE AND IMIDAZOPYRIDAZINE DERIVATIVES AS PROTEASE ACTIVATED RECEPTOR 4 (PAR4) INHIBITORS FOR TREATING PLATELET AGGREGATION

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Paragraph 00149; 00151, (2013/11/18)

The present invention provides imidazothiadiazole compounds of Formula (I); Wherein W,Y, R0, R2, R4, Ra, Rb, X1, X2, X3 and X4 are as defined herein,, or a stereoisomer, tautomer, pharmaceutically acceptable salt, prodrug ester or solvate form thereof, wherein all of the variables are as defined herein. These compounds are inhibitors of platelet aggregation and thus can be used as medicaments for treating or preventing thromboembolic disorders.

Bis (biaryl) compounds as inhibitors of leukotriene biosynthesis

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, (2008/06/13)

Compounds having the Formula I: STR1 are inhibitors of leukotriene biosynthesis. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating angina, cerebral spasm, glomerular nephritis, hepatitis, endotoxemia, uveitis, and allograft rejection and in preventing the formation of atherosclerotic plaques.

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