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Cyclopropanecarbonyl chloride, 3-ethenyl-2,2-dimethyl-, (1R,3R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84368-72-9

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84368-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84368-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,6 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84368-72:
(7*8)+(6*4)+(5*3)+(4*6)+(3*8)+(2*7)+(1*2)=159
159 % 10 = 9
So 84368-72-9 is a valid CAS Registry Number.

84368-72-9SDS

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 (1R,3R)-3-ethenyl-2,2-dimethylcyclopropane-1-carbonyl chloride

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:84368-72-9 SDS

84368-72-9Downstream Products

84368-72-9Relevant academic research and scientific papers

Photoreactions of γ,δ-unsaturated chromium carbene complexes

Moser, William H.,Hegedus, Louis S.

, p. 7873 - 7880 (2007/10/03)

A number of functionalized γ,δ-unsaturated chromium carbene complexes were synthesized, and their photochemistry was studied. Photolysis of carbene complexes 5 and 17 induced intramolecular [2 + 2] cycloaddition to afford cyclobutanones 6 and 18, respectively. If the photoreactions were not run in thoroughly degassed solvents, small amounts of lactones 7 and 19 were obtained as well. Cyclobutanones 6 and 18 were stable once isolated, but underwent an acid-catalyzed Pinacol rearrangement/hydrolysis transformation in acidic solution to afford novel α-hydroxy-substituted bicyclo[3.1.0]hexanone compounds 20 and 21. Photolysis of cyclopropyl carbene complex 28 induced a vinylcyclopropyl rearrangement involving the photogenerated ketene moiety to provide α-alkoxy cyclopentenone 29.

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