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3112-82-1

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3112-82-1 Usage

Appearance

White to off-white solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

a. Building block in the synthesis of other organic compounds
b. Production of pharmaceuticals and agrochemicals
c. Fragrance ingredient
d. Component in the manufacturing of dyes and pigments

Potential applications

a. Antioxidant
b. Anti-inflammatory agent

Industrial and research applications

Due to its unique molecular structure and properties, it has multiple applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 3112-82-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3112-82:
(6*3)+(5*1)+(4*1)+(3*2)+(2*8)+(1*2)=51
51 % 10 = 1
So 3112-82-1 is a valid CAS Registry Number.

3112-82-1SDS

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-(benzenesulfonyl)-1,3,5-trimethylbenzene

1.2 Other means of identification

Product number -
Other names 2,4,6-Trimethyldiphenylsulphone

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:3112-82-1 SDS

3112-82-1Relevant articles and documents

Hancock,Orszulik

, p. 3789 (1979)

Synthesis method of diaryl sulfone compound (by machine translation)

-

Paragraph 0007; 0017-0018; 0053-0055, (2019/12/31)

The invention discloses a synthesis method of a diaryl sulfone compound, wherein the, reaction equation of the series of N - diarylsulfone compounds is prepared by (NFSI) sulfonylating the aromatic hydrocarbon under the non-metal condition with the source of the, benzenesulfonyl group as the benzenesulfonyl group, and: the reaction equation is as follows. STR3, #, STR2, #, STR2, #, #, #, # STR2. # STR2# STR2# STR2, , STR2 STR2 STR2 N - # (NFSI) STR2# STR2 STR2 STR2, #, # STR1 STR8# STR2 STR1 STR8. AlCl R3 , FeCl3 The other precious, and metals of, other metals such as the precious metals of, the other noble metals not cause the environment, to pollute, the environment and are suitable for the concise and high-efficiency synthesis of. the diarylsulfone compounds, and have good application prospects in the fields of organic synthesis, drug research and development and the like. (by machine translation)

A practical synthesis of aryl sulfones via cross-coupling of sulfonyl hydrazides with aryltriazenes using copper/ionic liquid combination

Pandey, Anand Kumar,Kumar, Saurabh,Singh, Rahul,Singh, Krishna Nand

supporting information, p. 6704 - 6709 (2018/10/15)

A new and efficient approach adopting copper-catalyzed cross-coupling of sulfonyl hydrazides with aryltriazenes has been developed to synthesize aryl sulfones using Br?nsted acidic ionic liquid as promoter under ambient conditions. The process employs stable and easy to handle reacting partners, and is endowed with broad substrate scope.

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