68900-88-9 Usage
Uses
Used in Fragrance Industry:
(E)-6-Methylhept-3-en-1-ol is used as a fragrance ingredient for its aromatic properties, adding a pleasant and natural scent to various products such as soaps, shampoos, and perfumes.
Used in Flavor Manufacturing:
In addition to its application in the fragrance industry, (E)-6-Methylhept-3-en-1-ol is also utilized in the manufacture of flavors, enhancing the sensory experience of food and beverages.
Used as a Chemical Intermediate:
Furthermore, (E)-6-Methylhept-3-en-1-ol serves as a chemical intermediate in the synthesis of other compounds, contributing to the development of a wide range of products across different industries.
Natural Sources and Synthesis:
(E)-6-Methylhept-3-en-1-ol can be found in various natural sources, including flowers and fruits, and it can also be synthesized through chemical processes, making it accessible for a broad spectrum of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 68900-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,9,0 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68900-88:
(7*6)+(6*8)+(5*9)+(4*0)+(3*0)+(2*8)+(1*8)=159
159 % 10 = 9
So 68900-88-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-8(2)6-4-3-5-7-9/h3-4,8-9H,5-7H2,1-2H3/b4-3+
68900-88-9Relevant academic research and scientific papers
Alexakis, Alex,Hanaizi, Jezia,Jachiet, Denis,Normant, Jean-F.,Toupet, Loic
, p. 1271 - 1274 (1990)
Lithim dihydropyranyl or dihydrofuranyl triorganoaluminates react with cyclohexene oxide or benzaldehyde in the presence of BF3. OEt2, not by nucleophilic attack product 1, but by 1,2 migration of α substituent from Al to the ?-carbon, with concomitant reaction with the electrophile on the β-carbon, giving rise to product 2.
Preparation of unsaturated alcohols
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, (2008/06/13)
This invention relates to the preparation of unsaturated alcohols useful as flavor and fragrance compounds. More specifically, this invention relates to the preparation of predominately cis-unsaturated alcohols by reacting a cis-1-alkenylaluminum dialkyl compound with an epoxide compound followed by hydrolysis. The alkenyl moiety has one or more double bond carbon-to-carbon linkage and from 5 to 20 carbon atoms that can be optionally substituted with the substituents selected from alkyl and aromatic radicals having 1 to 12 carbon atoms.
