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3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethenyl)-, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81893-41-6

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81893-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81893-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,9 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81893-41:
(7*8)+(6*1)+(5*8)+(4*9)+(3*3)+(2*4)+(1*1)=156
156 % 10 = 6
So 81893-41-6 is a valid CAS Registry Number.

81893-41-6Relevant academic research and scientific papers

Process for making terpene esters

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Page/Page column 6, (2008/06/13)

A process for making terpene esters is disclosed. Reaction of a terpene alcohol with acetic anhydride in the presence of a high-boiling amine provides a terpene ester. Acetic acid, which is distilled from the reaction mixture as it forms can be recovered. The terpene ester is distilled from the high-boiling amine to provide a product that is substantially free of nitrogen-containing impurities. The reaction mixture can be reused for subsequent acylations. The simple, economical process gives high-quality terpene esters while avoiding waste-disposal issues of other common acylation procedures.

METAL-CATALYZED REARRANGEMENTS OF ALLYLIC ESTERS

Oehlschlager, A. C.,Mishra, P.,Dhami, S.

, p. 791 - 797 (2007/10/02)

It has been shown that Pd(CH3CN)2Cl2 catalyzes the rearrangement of allylic esters.Carbamates rearrange more rapidly than acetates which in turn rearrange more rapidly than carbonates.Allylic carbamates are more rapidly isomerized by Pd(CH3CN)2Cl2 than by Hg(OCOCF3)2.The rearrangement proceeds well except in cases where the central carbon of the allylic system is fully substituted.In contrast to the reported rearrangement of allylic carbamates by Hg2+ and previous reports of Pd2+-catalyzed rearrangements of allylic esters, this work showed the latter are extremely E specific; thus E allylic acetates yield equilibrium mixtures free of Z allylic isomers, under conditions in which Z allylic acetates are unreactive.This E specificity is applied to stereospecific 1,3-diene synthesis from bis E,Z-allylic acetates

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