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Acetic acid, (2-methylcyclohexylidene)-, methyl ester, (Z)- is a chemical compound with the molecular formula C10H16O2. It is an ester derivative of acetic acid, featuring a 2-methylcyclohexylidene group attached to the acetic acid moiety. The (Z)- configuration indicates the geometric arrangement of the double bond in the molecule, with the substituents on the same side of the double bond. Acetic acid, (2-methylcyclohexylidene)-, methyl ester, (Z)- is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and fragrances. It is an organic compound that can be synthesized through various chemical reactions and is characterized by its specific molecular structure and reactivity.

2208-95-9

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2208-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2208-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2208-95:
(6*2)+(5*2)+(4*0)+(3*8)+(2*9)+(1*5)=69
69 % 10 = 9
So 2208-95-9 is a valid CAS Registry Number.

2208-95-9SDS

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 methyl 2-(2-methylcyclohexylidene)acetate

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:2208-95-9 SDS

2208-95-9Relevant academic research and scientific papers

Stereoselective Formation of E- or Z-Exocyclic Alkenes via Radical Cyclization Reactions oof Acetylenic Esters

Lowinger, Timothy B.,Weiler, Larry

, p. 6099 - 6101 (2007/10/02)

The intramolecular cyclization of secondary alkyl radicals with α,β-alkynyl esters proceeds stereoselectively to give either E- or Z-exocyclic alkenes, depending upon the reaction conditions.

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