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2-Cyclohexene-1-methanol, 2,6,6-trimethyl-a-2-propenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28897-23-6

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28897-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28897-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,9 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28897-23:
(7*2)+(6*8)+(5*8)+(4*9)+(3*7)+(2*2)+(1*3)=166
166 % 10 = 6
So 28897-23-6 is a valid CAS Registry Number.

28897-23-6Relevant academic research and scientific papers

New preparation methods for α-damascone, γ-damascone, and β-damascenone using pyronenes

Boulin, Bertrand,Taran, Martine,Miguel, Bernadette Arreguy-San,Delmond, Bernard

, p. 2579 - 2591 (2008/02/10)

γ- and δ-Pyronenes are terpenic synthons easily available from myrcene. They are used as intermediates in the synthesis of α-damascone, γ-damascones, and β-damascenone. Copyright Taylor & Francis Group, LLC.

SYNTHESIS OF α-DAMASCONE AND 1-(2,6,6-TRIMETHYL-2-TETRAHYDROPYRANYL)-2-ALKEN-1-ONES

Erman, M. B.,Pribytkova, I. M.,Gulyi, S. E.,Bogomolova, O. A.,Cherkaev, G. V.,et al.

, p. 2294 - 2301 (2007/10/02)

α-Damascone was obtained by the reaction of α-cyclocitral with allyl bromide in the presence of zinc, followed by oxidation of the obtained alcohol with chromic acid to the ketone and isomerization of the latter with triethylamine as catalyst.The analogous synthesis of β-damascone from 1-(4,6,6-trimethyl-1,3-cyclohexadienyl)-2-buten-1-one was impossible on account of complications at the oxidation stage.The rearrangement of the acetylenic alcohols with polyvanadioorganosiloxane as catalyst led to 1-(2,6,6-trimethyl-2-tetrahydropyranyl)-2-alken-1-ones.

Alkenoyl-cyclohexadienes

-

, (2008/06/13)

New cycloaliphatic unsaturated ketones and their use as perfuming and odour-modifying agents in the manufacture of perfumes and perfumed products, and as flavouring and taste-modifying agents in the preparation of foodstuffs in general and imitation flavours for foodstuffs, beverages, animal feeds, pharmaceutical preparations and tobacco products. Methods for the preparation of said cycloaliphatic unsaturated ketones.

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