81176-43-4 Usage
Description
(S,E)-4-Phenyl-3-butene-2-ol, with the molecular formula C10H14O, is an unsaturated alcohol featuring a butene backbone with a phenyl group attached to one of the carbon atoms. This chemical compound is recognized for its pleasant floral aroma and can be found in various natural sources, such as certain flowers and plants. Its unique olfactory properties and versatility in organic synthesis contribute to its significance in the field of organic chemistry.
Uses
Used in Organic Synthesis:
(S,E)-4-Phenyl-3-butene-2-ol is used as a key intermediate in the synthesis of various organic compounds. Its structural features allow for a wide range of chemical reactions, making it a valuable building block in the creation of diverse molecules with potential applications in pharmaceuticals, materials science, and other areas.
Used in Fragrance Industry:
(S,E)-4-Phenyl-3-butene-2-ol is used as a fragrance ingredient for its unique floral scent. It contributes to the development of perfumes, colognes, and other aromatic products, enhancing their overall appeal and complexity.
Used in Flavor Industry:
In addition to its applications in fragrances, (S,E)-4-Phenyl-3-butene-2-ol is also utilized as a flavoring agent. Its pleasant aroma makes it suitable for the enhancement of flavors in the food and beverage industry, adding depth and character to various products.
Used in Aromatic Products:
(S,E)-4-Phenyl-3-butene-2-ol is employed in the production of other aromatic products, such as candles, air fresheners, and cleaning agents. Its incorporation into these products helps to create a more enjoyable and pleasant olfactory experience for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 81176-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,7 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81176-43:
(7*8)+(6*1)+(5*1)+(4*7)+(3*6)+(2*4)+(1*3)=124
124 % 10 = 4
So 81176-43-4 is a valid CAS Registry Number.
81176-43-4Relevant articles and documents
Chirality transfer during the [2,3]-sila-Wittig rearrangement and cyclopropanation reaction of optically active [(sec-allyloxy)silyl]lithiums
Kawachi,Maeda,Nakamura,Doi,Tamao
, p. 3143 - 3144 (2001)
-
Nickel-Catalyzed Enantioselective Hydroboration of Vinylarenes
Tran, Hai N.,Stanley, Levi M.
supporting information, p. 395 - 399 (2021/12/27)
The enantioselective hydroboration of vinylarenes catalyzed by a chiral, nonracemic nickel catalyst is presented as a facile method for generating chiral benzylic boronate esters. Various vinylarenes react with bis(pinacolato)diboron (B2pin2) in the presence of MeOH as a hydride source to form chiral boronate esters in up to 92% yield with up to 94% ee. The use of anhydrous Me4NF to activate B2pin2 is crucial for ensuring fast transmetalation to achieve high enantioselectivities.
Cobalt-Catalyzed Enantiospecific Dynamic Kinetic Cross-Electrophile Vinylation of Allylic Alcohols with Vinyl Triflates
Han, Guan-Yu,Kang, Shaolin,Liu, Xue-Yuan,Ma, Wei-Yuan,Pang, Xiaobo,Shu, Xing-Zhong
supporting information, p. 15930 - 15935 (2021/10/20)
Asymmetric cross-electrophile coupling has emerged as a promising tool for producing chiral molecules; however, the potential of this chemistry with metals other than nickel remains unknown. Herein, we report a cobalt-catalyzed enantiospecific vinylation
