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1121-24-0

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1121-24-0 Usage

Chemical Properties

Clear pale green to yellow liquid

Uses

2-Hydroxythiophenol can be used to increase blood-?free apoptosis inhibitor of macrophage (AIM)

General Description

2-Mercaptophenol (H2mp) is a 1,2-bidentate sulfur containing ligand. It exhibits versatile coordination modes in its ligation to the transition metal atoms.

Check Digit Verification of cas no

The CAS Registry Mumber 1121-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1121-24:
(6*1)+(5*1)+(4*2)+(3*1)+(2*2)+(1*4)=30
30 % 10 = 0
So 1121-24-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6OS/c7-5-3-1-2-4-6(5)8/h1-4,7-8H

1121-24-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L12519)  2-Hydroxythiophenol, 97%   

  • 1121-24-0

  • 1g

  • 430.0CNY

  • Detail
  • Alfa Aesar

  • (L12519)  2-Hydroxythiophenol, 97%   

  • 1121-24-0

  • 5g

  • 1436.0CNY

  • Detail
  • Aldrich

  • (465348)  2-Mercaptophenol  95%

  • 1121-24-0

  • 465348-1G

  • 671.58CNY

  • Detail
  • Aldrich

  • (465348)  2-Mercaptophenol  95%

  • 1121-24-0

  • 465348-5G

  • 2,341.17CNY

  • Detail

1121-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-HYDROXYTHIOPHENOL

1.2 Other means of identification

Product number -
Other names 2-sulfanylphenol

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:1121-24-0 SDS

1121-24-0Relevant articles and documents

-

Benoit,Bovet

, p. 97,102 (1938)

-

Copper(II)-Catalyzed Single-Step Synthesis of Aryl Thiols from Aryl Halides and 1,2-Ethanedithiol

Liu, Yajun,Kim, Jihye,Seo, Heesun,Park, Sunghyouk,Chae, Junghyun

supporting information, p. 2205 - 2212 (2015/07/27)

A highly efficient transition metal-catalyzed single-step synthesis of aryl thiols from aryl halides has been developed employing copper(II) catalyst and 1,2-ethanedithiol. The key features are use of readily available reagents, a simple operation, and relatively mild reaction conditions. This new protocol shows a broad substrate scope with excellent functional group compatibility. A variety of aryl thiols are directly prepared from aryl halides in high yields. Furthermore, the aryl thiols are used in situ for the synthesis of more advanced molecules such as diaryl sulfides and benzothiophenes.

Aromatic hydroxythiol synthesis using diazonium salts

-

, (2008/06/13)

A method for the preparation of aromatic hydroxythiols including oxidizing an aromatic aminothiol to form an aminodisulfide compound; forming a bis-diazonium salt of the aminodisulfide compound; and reacting the bis-diazonium salt with water to form an aromatic hydroxyldisulfide compound, which is then reduced to the hydroxythiol. New bis-diazonium aromatic disulfide compounds are also disclosed.

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