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Bicyclo[4.2.0]octa-2,4,7-triene, also known as bicyclo[4.2.0]octa-2,4,7-triene or simply "bicyclo", is a cyclic hydrocarbon with the molecular formula C8H8. It is a polycyclic aromatic hydrocarbon (PAH) consisting of two fused cyclohexane rings with a double bond between the two carbons that are not part of the fusion. Bicyclo[4.2.0]octa-2,4,7-triene is known for its unique structure and is often used as a precursor in the synthesis of various organic compounds. Bicyclo[4.2.0]octa-2,4,7-triene is a colorless liquid with a pungent odor and is insoluble in water but soluble in organic solvents. It is an important intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential health risks, it is essential to handle Bicyclo[4.2.0]octa-2,4,7-triene with proper safety measures.

4011-16-9

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4011-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4011-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4011-16:
(6*4)+(5*0)+(4*1)+(3*1)+(2*1)+(1*6)=39
39 % 10 = 9
So 4011-16-9 is a valid CAS Registry Number.

4011-16-9SDS

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 bicyclo(4.2.0)octa-2,4,7-triene

1.2 Other means of identification

Product number -
Other names Bicyclo[4.2.0]octa-2,4,7-triene

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:4011-16-9 SDS

4011-16-9Relevant academic research and scientific papers

1-Thia-3,4-diazolidine-2,5-dione Functionality: A Photochemical Synthon for the Azo Group

Squillacote, Michael,Felippis, James De

, p. 3564 - 3571 (2007/10/02)

The 1-thia-3,4-diazolidine-2,5-dione functional group was shown to yield azo compounds upon photolysis.This photoreaction when combined with the known ability of this group to react in a Diels-Alder fashion or as a dinucleophile toward alkylating agents greatly increases the utility of this functionality.The dual reactivity of this group was demonstrated in the synthesis of a number of 3,4-dialkyl-1-thia-3,4-diazolodone-2,5-diones.The photolysis of these compounds produced either thermally stable cyclic azo compounds or the decomposition products of thermally unstable azo compounds.

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