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Bicyclo[4.1.0]hept-2-ene, 7,7-bis(2,4,6-trimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87969-93-5

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87969-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87969-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,6 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87969-93:
(7*8)+(6*7)+(5*9)+(4*6)+(3*9)+(2*9)+(1*3)=215
215 % 10 = 5
So 87969-93-5 is a valid CAS Registry Number.

87969-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,7-bis(2,4,6-trimethylphenyl)bicyclo[4.1.0]hept-4-ene

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:87969-93-5 SDS

87969-93-5Downstream Products

87969-93-5Relevant academic research and scientific papers

Singlet and Triplet Dimesitylcarbene

Nazran, A. S.,Griller, D.

, p. 543 - 547 (2007/10/02)

The triplet states of essentially all diarylcarbenes react with substrates such as methanol or their parent diazo compounds both of which are thought to be specific quenchers for the singlet state.To rationalize these results, investigators have proposed that the singlet and triplet states of these carbenes are linked by efficient equilibria.In this kinetic study we have found that the singlet and triplet states of dimesitylcarbene exhibit quite distinct chemistries.The singlet state alone reacts with methanol, 1-propanol, and 1,3-cyclohexadiene, while the triplet carbene dimerizes to give olefin or, for example, reacts with oxygen.No evidence was found for reaction of the triplet carbene via the singlet manifold.Arguments are presented to explain the enhanced free energy difference between the spin states of this carbene and the relative persistence if its triplet.

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