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2-Vinyl-6,6-dimethylbicyclo[3.1.1]hept-2-ene is a chemical compound with the molecular formula C11H16. It is a colorless liquid with a pungent odor and is derived from the class of bicyclic compounds. 2-Vinyl-6,6-dimethylbicyclo[3.1.1]hept-2-ene is characterized by its unique structure, featuring a vinyl group attached to a bicyclo[3.1.1]heptane ring, which consists of seven carbon atoms arranged in a bridged ring system. The molecule also contains two methyl groups attached to the carbon atoms at positions 6 and 6, contributing to its stability and reactivity. 2-Vinyl-6,6-dimethylbicyclo[3.1.1]hept-2-ene is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatile chemical properties and potential for further functionalization.

473-00-7

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473-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 473-00-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 473-00:
(5*4)+(4*7)+(3*3)+(2*0)+(1*0)=57
57 % 10 = 7
So 473-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H16/c1-4-8-5-6-9-7-10(8)11(9,2)3/h4-5,9-10H,1,6-7H2,2-3H3

473-00-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethenyl-6,6-dimethylbicyclo[3.1.1]hept-3-ene

1.2 Other means of identification

Product number -
Other names 6,6-Dimethyl-2-vinylbicyclo<3.1.1>hept-2-ene

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:473-00-7 SDS

473-00-7Relevant academic research and scientific papers

PRODUCTS FROM SOLVOLYSIS OF 2-(2-TOSYLOXYETHYL)-6,6-DIMETHYLBICYCLOHEPT-2-ENE

Vyglazov, O. G.,Urbanovich, T. R.,Manukov, E. N.,Chuiko, V. A.,Udarov, B. G.

, p. 1896 - 1900 (2007/10/02)

The solvolysis of 2-(2-tosyloxyethyl)-6,6-dimethylbicyclohept-2-ene takes place with retention of the gem-dimethylcyclobutane ring of the substrate and is accompanied by simultaneous opening of the additional three-or four-membered ring in the reaction product.

Rearrangements of Pinane Derivatives. Part 91. 8,8-Dimethyltricyclo-2,5>nonan-2β-ol, a Tricyclic Pinane Derivative

Giddings, Rodney M.,Jones-Parry, Richard,Owen, Rawson,Whittaker, David

, p. 1525 - 1528 (2007/10/02)

Acetolysis of the toluene-p-sulphonate ester of 2-(2-hydroxyethyl)-6,6-dimethylbicyclohept-2-ene (nopol) (1; R = OH) gave a good yield of the acetate of the previously unknown tricyclic pinane derivative 8,8-dimethyltrycyclo2,5>n

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