6111-82-6 Usage
Description
[(E)-1-Hexenyl]benzene, also known as phenylhexene, is a chemical compound characterized by a hexenyl group attached to a benzene ring. This colorless liquid possesses a sweet, floral odor and is recognized for its diverse applications across various industries.
Uses
Used in the Food and Beverage Industry:
[(E)-1-Hexenyl]benzene is used as a flavoring agent to impart a pleasant fragrance and taste to a wide array of products. Its aromatic properties make it a valuable addition to the industry, enhancing the sensory experience of consumers.
Used in the Perfume and Cosmetics Industry:
Due to its sweet, floral scent, [(E)-1-Hexenyl]benzene is utilized as a key component in the production of perfumes and other cosmetic products. It contributes to the creation of captivating and long-lasting fragrances that are appreciated by consumers.
Used in the Pharmaceutical Industry:
[(E)-1-Hexenyl]benzene serves as an intermediate in the synthesis of various compounds within the pharmaceutical sector. Its chemical properties make it a versatile building block for developing new medications and therapies.
Used in the Chemical Industry:
Similarly, in the chemical industry, [(E)-1-Hexenyl]benzene is employed as an intermediate for synthesizing a range of compounds. Its adaptability and functional groups allow for its use in creating diverse chemical products, further expanding its utility and relevance in the market.
Check Digit Verification of cas no
The CAS Registry Mumber 6111-82-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,1 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6111-82:
(6*6)+(5*1)+(4*1)+(3*1)+(2*8)+(1*2)=66
66 % 10 = 6
So 6111-82-6 is a valid CAS Registry Number.
6111-82-6Relevant articles and documents
Ir-Catalyzed Remote Functionalization by the Combination of Deconjugative Chain-Walking and C-H Activation Using a Transient Directing Group
Tang, King Hung Nigel,Uchida, Kanako,Nishihara, Kazuki,Ito, Mamoru,Shibata, Takanori
supporting information, p. 1313 - 1317 (2022/02/23)
An Ir-catalyzed reaction of N-benzylideneanilines with functionalized alkenes such as α,β-unsaturated esters gave ortho-substituted benzaldehyde derivatives with a functional group at the remote position after acidic treatment. The present transformation
Recyclable and reusable PdCl2(PPh3)2/PEG-400/H2O system for the hydrophenylation of alkynes with sodium tetraphenylborate
Liu, Rong,Zhang, Tingli,Huang, Bin,Cai, Mingzhong
, p. 172 - 178 (2020/07/04)
A stable and efficient PdCl2(PPh3)2/PEG-400/H2O catalytic system for the hydrophenylation reaction of alkynes has been developed. In the presence of 3 mol% PdCl2(PPh3)2 and 2 equiv. of HOAc, the hydrophenylation of both terminal and internal alkynes with sodium tetraphenylborate proceeded smoothly in a mixture of PEG-400 and water at room temperature or 50 °C to afford a variety of phenyl-substituted alkenes in moderate to high yields. The isolation of the products was easily performed by extraction with petroleum ether, and the PdCl2(PPh3)2/PEG-400/H2O system could be readily recycled and reused six times without apparent loss of catalytic activity.
Selective hydroboration of equilibrating allylic azides
Liu, Ruzhang,Xu, Jun,Zhang, Yuanyuan
supporting information, p. 8913 - 8916 (2021/09/13)
The iridium(i)-catalyzed hydroboration of equilibrating allylic azides is reported to provide only the anti-Markovnikov product of alk-1-ene isomers in good yields and with good functional group tolerance.
