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Bicyclo[3.2.0]hept-2-en-6-one, 7,7-dimethyl-, also known as 7,7-dimethylbicyclo[3.2.0]hept-2-en-6-one, is a chemical compound with the molecular formula C9H12O. It is a cyclic ketone with a unique bicyclic structure, consisting of seven carbon atoms and two methyl groups attached to the seventh carbon. Bicyclo[3.2.0]hept-2-en-6-one,7,7-dimethyl- is an organic molecule that can be found in various natural products and is used in the synthesis of pharmaceuticals, fragrances, and other chemical compounds. Its chemical structure and properties make it an interesting target for research in organic chemistry and drug development.

767-85-1

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767-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 767-85-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 767-85:
(5*7)+(4*6)+(3*7)+(2*8)+(1*5)=101
101 % 10 = 1
So 767-85-1 is a valid CAS Registry Number.

767-85-1SDS

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 6,6-dimethylbicyclo[3.2.0]hept-3-en-7-one

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

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More Details:767-85-1 SDS

767-85-1Relevant academic research and scientific papers

Carbocyclic Analogues of Penicillin

Meth-Cohn, Otto,Reason, Andrew J.,Roberts, Stanley M.

, p. 90 - 92 (1982)

The synthesis of the title systems is described by cycloaddition of dimethylketen to cyclopentadiene, addition of hypobromous acid to the product and use of a nitrile-mediated rearrangement to give 4-cyano-6-exo-benzyloxy-3,3-dimethylbicycloheptan-2-one (5b) and its derivatives by further modification.

Synthesis of (3S,4R)-Eldanolide and (5S,12R)-Leukotriene-B4 through Photolysis of Optically Active Hydroxy-7,7-dimethylbicycloheptanones

Davies, H. Geoff,Roberts, Stanley M.,Wakefield, Basil J.,Winders, John A.

, p. 1166 - 1168 (2007/10/02)

Photoisomerisation of 3-hydroxy-7,7-dimethylbicycloheptan-6-ones is the key step in a new route to the pheromone eldanolide while leukotriene-B4 is available through a photolytic retro reaction of 2-hydroxy-7,7-dimethylbicycloheptan-6-ones.

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