125872-62-0 Usage
Description
(E)-3-[4-(methylsulfanyl)phenyl]prop-2-en-1-ol, also known as 4-Methylthio-β-methylstyrene, is an organic compound characterized by its molecular formula C10H12OS. It is a colorless to pale yellow liquid with a distinct odor and is recognized for its significant role in various industrial applications and chemical processes.
Uses
Used in Flavor and Fragrance Industry:
(E)-3-[4-(methylsulfanyl)phenyl]prop-2-en-1-ol is utilized as a key component in the production of flavors and fragrances, adding unique scents and enhancing the sensory experience of various products.
Used in Pharmaceutical Industry:
(E)-3-[4-(methylsulfanyl)phenyl]prop-2-en-1-ol serves as an essential intermediate in the manufacturing of pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Industry:
(E)-3-[4-(methylsulfanyl)phenyl]prop-2-en-1-ol is also employed in the production of agrochemicals, playing a vital role in the development of agricultural products that can improve crop yield and protect plants from pests.
Used as an Intermediate in Organic Synthesis:
(E)-3-[4-(methylsulfanyl)phenyl]prop-2-en-1-ol is widely used as an intermediate in organic synthesis, enabling the creation of a diverse range of chemical products and materials.
Precaution:
Due to its potential health hazards, including the risk of skin and eye irritation upon contact, (E)-3-[4-(methylsulfanyl)phenyl]prop-2-en-1-ol should be handled with care to ensure safety during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 125872-62-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,7 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125872-62:
(8*1)+(7*2)+(6*5)+(5*8)+(4*7)+(3*2)+(2*6)+(1*2)=140
140 % 10 = 0
So 125872-62-0 is a valid CAS Registry Number.
125872-62-0Relevant articles and documents
Strong acid-catalyzed electrophilic ring expansion of oxetanes and sulfoxonium ylides
Xie, Wenlai,Xu, Jiaxi,Yuan, Wenhao
, (2021/06/28)
A strong protic acid-catalyzed electrophilic ring expansion of oxetanes into trans-2,3-disubstituted tetrahydrofuran derivatives using sulfoxonium ylides has been developed. This reaction produces functionalized trans-2,3-disubstituted tetrahydrofuran derivatives stereospecifically by using safe and stable sulfoxonium ylides without metal catalysts and the protection of inert gas.
Integrating Allyl Electrophiles into Nickel-Catalyzed Conjunctive Cross-Coupling
Derosa, Joseph,Engle, Keary M.,Gallagher, Timothy J.,Li, Zi-Qi,Liu, Peng,Tran, Van T.
supporting information, p. 7029 - 7034 (2020/03/23)
Allylation and conjunctive cross-coupling represent two useful, yet largely distinct, reactivity paradigms in catalysis. The union of these two processes would offer exciting possibilities in organic synthesis but remains largely unknown. Herein, we repor
A facile and efficient asymmetric synthesis of florfenicol
Li, Feng,Wang, Zhong-Hua,Zhao, Lei,Chen, Fen-Er
scheme or table, p. 2883 - 2885 (2012/01/11)
A facile and efficient enantioselective synthesis of flor-fenicol starting from commercially available 4-methylthiobenzaldehyde is described. Key features of the synthesis include a one-step oxidation of allyl and thioether groups in allylic alcohol to form (2S,3S)-epoxide under Sharpless epoxidation conditions and a highly efficient conversion of (1R,2R)-azide into amino alcohol via debenzylation and reduction of an azido moiety in one-pot operation. Georg Thieme Verlag Stuttgart. New York.
