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5-(2,6,6-trimethylcyclohex-1-enyl)penta-2,4-dien-1-ol is a complex organic compound with the molecular formula C14H22O. It features a cyclohexene ring with three methyl groups at positions 2, 6, and 6, and a pentadienol chain with a hydroxyl group at the 1-position. This chemical is characterized by its unique structure, which includes a conjugated diene system in the pentadienol chain and a cyclohexene ring. It is an example of a terpene, which are a large and diverse class of organic compounds derived from isoprene units, and are often found in plants and essential oils. The specific structure of 5-(2,6,6-trimethylcyclohex-1-enyl)penta-2,4-dien-1-ol may endow it with particular chemical properties and potential applications in various fields, such as fragrances, pharmaceuticals, or as a chemical intermediate.

4808-04-2

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4808-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4808-04-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4808-04:
(6*4)+(5*8)+(4*0)+(3*8)+(2*0)+(1*4)=92
92 % 10 = 2
So 4808-04-2 is a valid CAS Registry Number.

4808-04-2Relevant articles and documents

Palladium-catalyzed coupling reaction of an enol nonaflate with (vinyl)tributylstannanes and acetylenes: A highly stereoselective synthesis of 8,18-13C2-labeled retinal

Wada, Akimori,Ieki, Yasuhiro,Nakamura, Saeko,Ito, Masayoshi

, p. 1581 - 1588 (2007/10/03)

Here we report that enol nonaflates exhibit higher reactivity than the corresponding enol triflates in palladium-catalyzed cross-coupling reactions with various (vinyl)tributylstannanes and acetylenes. We also highlight the reaction of a vinyl nonaflate,

Palladium catalyzed coupling reaction of an enol nonaflate with (vinyl)tributylstannanes and acetylenes

Wada, Akimori,Ieki, Yasuhiro,Ito, Masayoshi

, p. 1061 - 1064 (2007/10/03)

A novel method for a stereoselective synthesis of trienes and dienynes was developed by palladium catalyzed cross coupling reactions of an enol nonaflate with (vinyl)tributylstannanes and acetylenes in good to excellent yields. Here, the enol nonaflate ex

Preparation of 11,14-epoxy-bridged and isomeric chain-demethylated retinals. 13-Demethyl-11,14-epoxy-, 9-demethyl-, 13-demethyl- and 9,13-bisdemethyl-retinals

Broek, A. D.,Muradin-Szweykowska, M.,Courtin, J. M. L.,Lugtenburg, J.

, p. 46 - 51 (2007/10/02)

9-Cis- and all-trans-13-demethyl-11,14-epoxyretinyl acetate were prepared via a Wittig coupling between β-ionylidenetriphenylphosphonium bromide (1) and 5-(acetoxymethyl)furfural.Saponification of these acetates, subsequent oxidation and HPLC separation a

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