64576-90-5 Usage
Description
(2E,4E)-nona-2,4-dien-1-ol is a primary alcohol with the molecular formula C9H16O. It is a colorless liquid with a fruity odor and is commonly found in various fruits and flowers. This chemical compound contains a long chain of nine carbon atoms with two double bonds at the 2nd and 4th positions.
Uses
Used in Perfume and Flavor Industry:
(2E,4E)-nona-2,4-dien-1-ol is used as a key ingredient in the production of perfumes and flavors due to its pleasant and fruity odor. Its natural occurrence in fruits and flowers adds to its appeal as a fragrance and flavoring agent.
Used in Organic Synthesis:
(2E,4E)-nona-2,4-dien-1-ol is also used in the synthesis of various organic compounds. Its unique structure with two double bonds allows for versatile chemical reactions, making it a valuable building block in organic chemistry.
Used in Pharmaceutical Research:
(2E,4E)-nona-2,4-dien-1-ol has been studied for its potential pharmaceutical properties. Its natural occurrence and pleasant odor make it a promising candidate for further research and development in the pharmaceutical industry.
Used as a Natural Insect Repellent:
(2E,4E)-nona-2,4-dien-1-ol has been investigated for its potential as a natural insect repellent. Its ability to deter insects without the use of harsh chemicals makes it an attractive option for eco-friendly pest control solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 64576-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,7 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64576-90:
(7*6)+(6*4)+(5*5)+(4*7)+(3*6)+(2*9)+(1*0)=155
155 % 10 = 5
So 64576-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-2-3-4-5-6-7-8-9-10/h5-8,10H,2-4,9H2,1H3/b6-5+,8-7+
64576-90-5Relevant articles and documents
Total synthesis of micropine and epimicropine
Bayquen, Aristea V.,Read, Roger W.
, p. 13467 - 13482 (1996)
The enantioselective total synthesis of micropine, an unusual 2,6-disubstituted piperidine alkaloid, and epimicropine, through mercuric trifluoroacetate-catalysed intramolecular alkenylamide cyclisation is described. The synthesis proceeds from L-serine and affords material of the same positive sign of optical rotation as the natural product thereby confirming the absolute stereochemistry of micropine.
Total synthesis of a piperidine alkaloid, microcosamine A
Raji Reddy, Chada,Latha, Bellamkonda,Warudikar, Kamalkishor,Singarapu, Kiran Kumar
, p. 251 - 258 (2015/12/30)
The first asymmetric total synthesis of a new natural piperidine alkaloid, microcosamine A, has been accomplished from d-serine and d-methyl lactate as chiral pool starting materials. Key features of the strategy include the utility of Horner-Wadsworth-Emmons reaction, Luche reduction, intramolecular carbamate N-alkylation to form the piperidine framework and Julia-Kocienski olefination to install the triene side-chain.
A short synthesis of conjugated unsaturated alcohols
Kazmaier, Uli
, p. 1491 - 1496 (2007/10/03)
Isomerization of acetylenic pentafluorophenyl esters in the presence of phosphines gives rise to activated dienoic esters, which can be reduced directly in a simple one pot procedure to the corresponding conjugated unsaturated alcohols 6-10. The higher reactivity of the pentafluorophenyl esters in comparison to alkyl esters allows their selective isomerization.
