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55214-86-3

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55214-86-3 Usage

General Description

o-(Phenylthio)phenol, also known as 2-Phenylthiophenol, is a chemical compound with the molecular formula C12H10OS. It belongs to the class of organic compounds known as biaryls, which contain two aromatic rings connected by a single bond. This chemical is solid in its physical state and appears in a pale yellow to deep yellow colour. It is typically used for various chemical syntheses in the field of organic chemistry, often serving as a building block in the pharmaceutical industry. It's important to handle this substance with care as it can cause skin and eye irritation and may be harmful if ingested or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 55214-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,1 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55214-86:
(7*5)+(6*5)+(5*2)+(4*1)+(3*4)+(2*8)+(1*6)=113
113 % 10 = 3
So 55214-86-3 is a valid CAS Registry Number.

55214-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylsulfanylphenol

1.2 Other means of identification

Product number -
Other names 2-(phenylthio)phenol

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:55214-86-3 SDS

55214-86-3Relevant articles and documents

CONFORMATIONAL CONSEQUENCES OF INTRAMOLECULAR HYDROGEN BONDING BY OH TO THE DIRECTIONAL LONE-PAIR OF SULFUR IN DERIVATIVES OF METHYL PHENYL SULFIDE, DIPHENYL SULFIDE, AND DIPHENYL DISULFIDE

Schaefer, Ted,Salman, Salman R.,Wildman, Timothy A.,Clark, Peter D.

, p. 342 - 348 (1982)

Complete spectral parameters for the 1H nmr spectra of 2-hydroxyphenyl methyl sulfide, 2, 2-hydroxyphenyl phenyl sulfide, 3, bis(2-hydroxy-3-tert-butyl-5-methylphenyl) sulfide, 4, and bis(2-hydroxyphenyl)disulfide, 5, are reported for CCl4 solu

Achieving Nickel Catalyzed C-S Cross-Coupling under Mild Conditions Using Metal-Ligand Cooperativity

Sikari, Rina,Sinha, Suman,Das, Siuli,Saha, Anannya,Chakraborty, Gargi,Mondal, Rakesh,Paul, Nanda D.

, p. 4072 - 4085 (2019/04/01)

A simple and efficient approach of C-S cross-coupling of a wide variety of (hetero)aryl thiols and (hetero)aryl halides under mild conditions, mostly at room temperature, catalyzed by well-defined singlet diradical Ni(II) catalysts bearing redox noninnocent ligands is reported. Taking advantage of ligand centered redox events, the high-energetic Ni(0)/Ni(II) or Ni(I)/Ni(III) redox steps were avoided in the catalytic cycle. The cooperative participation of both nickel and the coordinated ligands during oxidative addition/reductive elimination steps allowed us to perform the catalytic reactions under mild conditions.

SULFONIUM COMPOUND, RESIST COMPOSITION, AND PATTERN FORMING PROCESS

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Paragraph 0172-0173, (2018/04/20)

A sulfonium compound having formula (1) is provided wherein R1, R2 and R3 are a C1-C20 monovalent hydrocarbon group which may contain a heteroatom, p=0-5, q=0-5, and r=0-4. A resist composition comprising the sulfonium compound is processed by lithography to form a resist pattern with improved LWR and pattern collapse.

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