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3756-33-0

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3756-33-0 Usage

Type of compound

Aromatic hydrocarbon

Structure

Three phenyl rings connected by carbon-carbon double bonds

Methyl group positions

2 and 5 on the central phenyl ring

Potential use in organic electronics

Unique electronic and optical properties

Building block for functional materials

Unique electronic and optical properties

Investigated for liquid crystal applications

Potential benefits in the field of liquid crystals

Precursor for the synthesis of other organic compounds

Can be used as a starting material for creating other organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 3756-33-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3756-33:
(6*3)+(5*7)+(4*5)+(3*6)+(2*3)+(1*3)=100
100 % 10 = 0
So 3756-33-0 is a valid CAS Registry Number.

3756-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2',5-DIMETHYL-4-TERPHENYL

1.2 Other means of identification

Product number -
Other names 2,5-DIPHENYL-4-XYLENE

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:3756-33-0 SDS

3756-33-0Downstream Products

3756-33-0Relevant articles and documents

Photochemical (Hetero-)Arylation of Aryl Sulfonium Salts

Zhao, Yue,Yu, Congjun,Liang, Wenjing,Patureau, Frederic W.

, p. 6232 - 6236 (2021/08/23)

The construction of (hetero)biaryls, which are ubiquitous scaffolds among medical substances, functional materials, and agrochemicals, constitutes a key application of cross-coupling methods. However, these usually require multiple synthetic steps. Herein, we report a simple photoinduced and catalyst-free C-H/C-H (hetero)arylation cross-coupling through aryl thianthrenium salts, which are formed site-selectively by direct C-H functionalization. The key to this approach is the UV-light, which can disrupt the C-S bond to form thianthrene radical cations and aryl radicals.

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