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Cis-chrysanthemyl alcohol, also known as cis-3-hexen-1-ol, is a naturally occurring organic compound found in various plants, particularly in the flowers of chrysanthemums. It is a colorless liquid with a strong, green, and herbaceous odor, and is an important component in the fragrance industry due to its ability to mimic the scent of freshly cut grass. This alcohol is also used in the production of perfumes, soaps, and other cosmetic products, as well as in the flavoring industry to add a natural, green note to food products. Cis-chrysanthemyl alcohol is synthesized through various chemical processes, and its safety and environmental impact are considered to be low, making it a widely used and versatile chemical in the fragrance and flavor industries.

2861-26-9

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2861-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2861-26-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,6 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2861-26:
(6*2)+(5*8)+(4*6)+(3*1)+(2*2)+(1*6)=89
89 % 10 = 9
So 2861-26-9 is a valid CAS Registry Number.

2861-26-9Relevant academic research and scientific papers

STRUCTURE OF THE STABLE CARBOCATION FROM CHRYSANTHEMYL ALCOHOLS

Korchagina, D. V.,Tatarova, L. E.,Gatilov, Yu. V.,Barkhash, V. A.

, p. 85 - 90 (2007/10/02)

An error was found in the previously described structure for the stable ion generated from trans- and cis-chrysanthemyl alcohols in fluorosulfonic acid.The real structure of the carbocation and its "quenching" product was determined.The reasons for the difference in the rearrangements in various media are discussed.

Studies of Chrysanthemic Acid Derivatives: Catalyses Reactions of 3-(2-Hydroxymethyl-3,3-dimethylcyclopropyl)-2-methylpropanol and Formation of a Novel Eight-membered Cyclic Sulphite

Crammer, Bernard,Goldschmidt, Zeev,Ikan, Raphael,Cohen, Shmuel

, p. 887 - 891 (2007/10/02)

Acid catalysed reaction of the cyclopropanediol (3) derived from cis-chrysanthemic acid cis-(1) afforded, depending on the reaction conditions, 3-vinyl-2,2,5,5-tetramethyltetrahydrofuran (4) and 4,4,7,7-tetramethyl-3-oxabicycloheptane (5).On treatment with thionyl chloride-pyridine complex there was obtained in addition the eight-membered cyclic sulphite, 6,6,9,9-tetramethyl-3,5-dioxa-4-thiabicyclononane 4-oxide (6).X-Ray analysis confirms a boat-chair conformation with the S=O group trans to the cyclopropane ring in an equatorial situation.Thermal reaction of (6) gave either (4) or a mixture of (5), cis-chrysanthemol (7), and cis-isochrysanthemol (8).

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