89929-82-8

Basic information

• Product Name: (3-THIEN-3-YLPHENYL)METHANOL
• Synonyms: [3-(3-THIENYL)PHENYL]METHANOL;(3-THIEN-3-YLPHENYL)METHANOL;AKOS BAR-1378;RARECHEM AL BD 1417;(3-Thien-3-ylphenyl)methanol 97%;(3-(Thiophen-3-yl)phenyl)methanol
• CAS NO: 89929-82-8
• Molecular Formula: C11H10OS
• Molecular Weight: 190.26
• Mol File: 89929-82-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 88-90
• Boiling Point: 306.7 °C at 760 mmHg
• Flash Point: 139.3 °C
• Appearance: /
• Density: 1.204 g/cm³
• Vapor Pressure: 0.000331mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: (3-THIEN-3-YLPHENYL)METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (3-THIEN-3-YLPHENYL)METHANOL(89929-82-8)
• EPA Substance Registry System: (3-THIEN-3-YLPHENYL)METHANOL(89929-82-8)

Safety Data

• Hazardous Substances Data: 89929-82-8(Hazardous Substances Data)

Usage

General Description

(3-Thien-3-ylphenyl)methanol is a chemical compound that belongs to the class of aryl alkyl alcohols. It is a white solid substance with a molecular formula of C13H12OS and a molecular weight of 220.3 g/mol. (3-Thien-3-ylphenyl)methanol is used in the synthesis of pharmaceuticals and organic compounds. It is also used in the preparation of other chemicals, such as insecticides and pesticides. Additionally, (3-Thien-3-ylphenyl)methanol has potential applications in the field of material science, particularly in the development of polymers and specialty chemicals. Overall, this compound has a diverse range of uses in the chemical industry.

InChI:InChI=1/C11H10OS/c12-7-9-2-1-3-10(6-9)11-4-5-13-8-11/h1-6,8,12H,7H2

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Relevant articles and documents

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

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

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.

Heterocyclic substituted benzyl alcohol, insecticidal ester derivatives, and intermediates

Disclosed and exemplified are insecticidal and acaricidal optionally substituted furylbenzyl, thienylbenzyl, pyrazinylbenzyl, or pyridinzylbenzyl esters of the pyrethroid acids, novel pyrethroid alcohols and other intermediates, and compositions, a method of use and a process for preparation of the esters.