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28864-95-1

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28864-95-1 Usage

General Description

Biphenyl, 4-(4-methylcyclohexyl)-, cis- is a chemical compound with the molecular formula C19H22. It is a cis isomer of 4-(4-methylcyclohexyl)biphenyl, and it is often used in the production of various polymers and plastics. Biphenyl, 4-(4-methylcyclohexyl)-, cis- is a white crystalline solid with a molecular weight of 250.377 g/mol. It is mainly used as a raw material for the synthesis of liquid crystals and organic electronic materials. Additionally, it is also used in the manufacturing of pharmaceuticals and agrochemicals due to its stability and chemical properties. As a chemical compound, it is important to handle it with proper care and follow safety guidelines for its usage and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 28864-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,6 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28864-95:
(7*2)+(6*8)+(5*8)+(4*6)+(3*4)+(2*9)+(1*5)=161
161 % 10 = 1
So 28864-95-1 is a valid CAS Registry Number.

28864-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Biphenyl, 4-(4-methylcyclohexyl)-, cis-

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:28864-95-1 SDS

28864-95-1Upstream product

28864-95-1Downstream Products

28864-95-1Relevant articles and documents

Efficient cross-coupling of secondary alkyltrifluoroborates with aryl chlorides-reaction discovery using parallel microscale experimentation

Dreher, Spencer D.,Dormer, Peter G.,Sandrock, Deidre L.,Molander, Gary A.

supporting information; body text, p. 9257 - 9259 (2009/02/02)

Microscale parallel experimentation was used to discover three catalyst systems capable of coupling secondary organotrifluoroborates with sterically and electronically demanding aryl chlorides and bromides. The ensuing results represent the first comprehensive study of alkylboron coupling to aryl chlorides and, in particular, using secondary alkylboron partners. A ligand-dependent β-hydride elimination/reinsertion mechanism was implicated in the cross-coupling of more hindered substrates, leading to isomeric mixtures of coupled products in some cases. Copyright

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