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68480-27-3

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68480-27-3 Usage

Description

2-Undecenylacetate, also known as 2-Undecenyl acetate or undec-2-en-1-yl acetate, is a colorless to pale yellow liquid chemical compound with a fruity, floral, and slightly sweet odor. It is commonly used in the manufacturing of perfumes and fragrances and is naturally found in many fruits and flowers.

Uses

Used in Fragrance Industry:
2-Undecenylacetate is used as a key ingredient in the creation of a wide range of scents, including jasmine, gardenia, and tropical fruit fragrances. Its natural presence in fruits and flowers contributes to its ability to enhance and mimic these scents in perfumes and other fragrance products.
Used in Flavor Industry:
2-Undecenylacetate is used as a flavoring agent in food products to impart a fruity taste. Its natural fruity aroma makes it a suitable addition to various food items, enhancing their flavor profiles and providing a pleasant sensory experience for consumers.
Used in Cosmetics and Food Products:
2-Undecenylacetate is considered safe for use in cosmetics, fragrances, and food products when used in accordance with established guidelines and regulations. Its safety profile and versatile applications make it a valuable component in various consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 68480-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,8 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68480-27:
(7*6)+(6*8)+(5*4)+(4*8)+(3*0)+(2*2)+(1*7)=153
153 % 10 = 3
So 68480-27-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O2/c1-3-4-5-6-7-8-9-10-11-12-15-13(2)14/h10-11H,3-9,12H2,1-2H3/b11-10+

68480-27-3Downstream Products

68480-27-3Relevant articles and documents

Towards Sustainable Catalysis – Highly Efficient Olefin Metathesis in Protic Media Using Phase Labelled Cyclic Alkyl Amino Carbene (CAAC) Ruthenium Catalysts

Nagyházi, Márton,Turczel, Gábor,Balla, áron,Szálas, Gábor,Tóth, Imre,Gál, Gyula Tamás,Petra, Bombicz,Anastas, Paul T.,Tuba, Róbert

, p. 1953 - 1957 (2020/02/15)

New generations of Hoveyda and bis-carbene type of ruthenium-based olefin metathesis catalysts (10 and 12), containing cationic cyclic alkyl amino carbene (CAAC) ligands, have been synthetized. The catalysts show exceptional stability and activity in environmentally benign, protic media. Various olefin metatheses reactions of OH functionalized feedstock (e. g. RCM, ROMP CM) can be carried out at as low as 0.05 mol % catalyst loading in methanol, isopropanol, water or methanol/water solvent mixture, accomplishing the lowest applied catalyst loading reported so far in these media. The facile olefin metathesis of renewable feedstocks including phospholipids (23) and vegetable oils (20) in protic media has also been demonstrated.

Highly Regioselective Palladium-Catalyzed Carboxylation of Allylic Alcohols with CO2

Mita, Tsuyoshi,Higuchi, Yuki,Sato, Yoshihiro

supporting information, p. 16391 - 16394 (2015/11/09)

Various allylic alcohols were carboxylated in the presence of a catalytic amount of PdCl2 and PPh3 using ZnEt2 as a stoichiometric transmetalation agent under a CO2 atmosphere (1atm). This carboxylation proceeded in a highly regioselective manner to afford branched carboxylic acids predominantly. The β,γ-unsaturated carboxylic acid thus obtained was successfully converted into an optically active γ-butyrolactone, a known intermediate of (R)-baclofen.

Metathesis of renewable raw materials - Influence of ligands in the indenylidene type catalysts on self-metathesis of methyl oleate and cross-metathesis of methyl oleate with (Z)-2-butene-1,4-diol diacetate

Kajetanowicz, Anna,Sytniczuk, Adrian,Grela, Karol

supporting information, p. 1579 - 1585 (2014/03/21)

The influence of different N-heterocyclic carbene (NHC) and other neutral ligands on the outcome of the cross-metathesis reaction of methyl oleate with (Z)-2-butene-1,4-diol diacetate and self-metathesis of methyl oleate was studied for a series of indenylidene type Ru catalysts.

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