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3111-81-7

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3111-81-7 Usage

Chemical structure

1,1'-Biphenyl, 3,3'-diphenoxyis a chemical compound with two benzene rings connected by a single bond, and each ring has a diphenoxy substitution at the 3 and 3' positions.

Building block

It is commonly used as a building block for the synthesis of various organic compounds.

Applications

It finds applications in the production of pharmaceuticals, agrochemicals, and materials science.

Potential

It is known for its potential as a useful starting material for the creation of new molecules with diverse properties and functions.

Intermediate

It is considered to be a key intermediate in the production of specialty chemicals and advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 3111-81-7 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 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3111-81:
(6*3)+(5*1)+(4*1)+(3*1)+(2*8)+(1*1)=47
47 % 10 = 7
So 3111-81-7 is a valid CAS Registry Number.

3111-81-7SDS

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 3,3'-diphenoxybiphenyl

1.2 Other means of identification

Product number -
Other names -

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:3111-81-7 SDS

3111-81-7Upstream product

3111-81-7Downstream Products

3111-81-7Relevant articles and documents

THE REACTION OF PYRITE WITH DIPHENYL ETHER

Smith, Peter A. S.,Munavu, Raphael M.,Gilbertson, Scott R.

, p. 2949 - 2952 (2007/10/02)

Diphenyl ether is converted into diphenyl sulfide (largely), dibenzofuran, phenoxybiphenyls, diphenoxybiphenyls, and several other sulfur-containing compounds by reaction with pyrite at 350-360 deg C.

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