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5,6-dimethylidenecyclohexa-1,3-diene is an organic compound with the molecular formula C8H10. It is a conjugated diene, featuring a cyclohexane ring with two methyl groups attached to the 5th and 6th carbon atoms, and a carbon-carbon double bond between the 1st and 3rd carbon atoms. 5,6-dimethylidenecyclohexa-1,3-diene is known for its unique chemical properties, such as its reactivity in Diels-Alder reactions, which are important in organic synthesis for forming six-membered rings. The structure of 5,6-dimethylidenecyclohexa-1,3-diene contributes to its stability and reactivity, making it a valuable intermediate in the synthesis of various pharmaceuticals and other organic compounds.

32714-83-3

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32714-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32714-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,1 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32714-83:
(7*3)+(6*2)+(5*7)+(4*1)+(3*4)+(2*8)+(1*3)=103
103 % 10 = 3
So 32714-83-3 is a valid CAS Registry Number.

32714-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name m-xylylene diradical

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:32714-83-3 SDS

32714-83-3Downstream Products

32714-83-3Relevant academic research and scientific papers

Matrix isolation, spectroscopic characterization, and photoisomerization of m-xylylene

Neuhaus, Patrik,Grote, Dirk,Sander, Wolfram

, p. 2993 - 3000 (2008/09/18)

A new efficient synthesis of m-xylylene 1 is reported. The diradical 1 was trapped in argon matrices at 10 K and characterized by IR, UV-vis, and EPR spectroscopy. The syntheses reported before only allowed generation of 1 in organic glasses, and the spec

The mechanism of formation of m-xylylene type biradicals produced by photolysis of polymethyl benzenes or dihalomethyl benzenes

Haider,Migirdicyan,Platz,Soundararajan,Despres

, p. 733 - 738 (2007/10/02)

The mechanism of formation of the mesitylylene biradical (3) produced by short-wavelength photolysis of matrix-isolated mesitylene (1) has been investigated. The data rule out a mechanism involving the sequential formation of the biradical 3 via photolysi

Recent Studies of Meta-Xylylene and a Diaza Derivative

Haider, K. W.,Migirdicyan, E.,Platz, M. S.,Soundararajan, N.,Despres, A.

, p. 85 - 98 (2007/10/02)

A new photochemical precursor to meta-xylylene is reported and its mechanism of action is discussed.A diaza derivative of meta-xylylene is also reported.

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