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85553-54-4

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85553-54-4 Usage

General Description

(3-Pyrid-3-ylphenyl)methanol is a chemical compound with the molecular formula C13H11NO. It is a white solid that is insoluble in water but soluble in organic solvents. (3-PYRID-3-YLPHENYL)METHANOL is used primarily in the field of pharmaceuticals and agrochemicals as a building block for the synthesis of various biologically active molecules. It can also act as a ligand in coordination chemistry, forming complexes with metal ions. Additionally, (3-pyrid-3-ylphenyl)methanol has been studied for its potential use in organic light-emitting diodes (OLEDs) due to its attractive light-emitting properties. Overall, this compound has a wide range of potential applications in various industries due to its versatile chemical and physical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 85553-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,5,5 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85553-54:
(7*8)+(6*5)+(5*5)+(4*5)+(3*3)+(2*5)+(1*4)=154
154 % 10 = 4
So 85553-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO/c14-9-10-3-1-4-11(7-10)12-5-2-6-13-8-12/h1-8,14H,9H2

85553-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-pyridin-3-ylphenyl)methanol

1.2 Other means of identification

Product number -
Other names -

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:85553-54-4 SDS

85553-54-4Downstream Products

85553-54-4Relevant articles and documents

Site-Selective Switching Strategies to Functionalize Polyazines

Dolewski, Ryan D.,Fricke, Patrick J.,McNally, Andrew

supporting information, p. 8020 - 8026 (2018/06/01)

Many drug fragments and therapeutic compounds contain multiple pyridines and diazines. Developing site-selective reactions where specific C-H bonds can be transformed in polyazine structures would enable rapid access to valuable derivatives. We present a study that addresses this challenge by selectively installing a phosphonium ion as a versatile functional handle. Inherent factors that control site-selectivity are described along with mechanistically driven approaches for site-selective switching, where the C-+PPh3 group can be predictably installed at other positions in the polyazine system. Simple protocols, readily available reagents, and application to complex drug-like molecules make this approach appealing to medicinal chemists.

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

-

Paragraph 00132; 00134, (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.

Pd-mediated C-C and C-S bond formation on solid support: A scope and limitations study

Wendeborn, Sebastian,Berteina, Sabine,Brill, Wolfgang K.-D.,De Mesmaeker, Alain

, p. 671 - 675 (2007/10/03)

The scope and limitations of Pd(0)-mediated coupling reactions between aromatic halides linked to a polystyrene resin and boronic acid derivatives (Suzuki coupling), aromatic and vinylic tin compounds (Stille coupling), as well as thiols are reported. For all reactions, conditions were optimized and evaluated with various reagents. In many cases, upon cleavage from the solid support, products were obtained in excellent yields. In most cases, the optimized reaction conditions are superior to those previously reported in the literature.

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