19819-98-8 Usage
Description
2-METHYLPHENETHYL ALCOHOL, also known as 2-phenyl-1-butanol, is an organic compound characterized by its clear, colorless liquid appearance. It is an aromatic alcohol with a distinctive chemical structure, featuring a phenyl group attached to a butyl chain.
Uses
Used in Chemical Synthesis:
2-METHYLPHENETHYL ALCOHOL is used as a synthetic building block for the creation of various chemical compounds. Its unique structure allows it to be a versatile component in the synthesis of pharmaceuticals, fragrances, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-METHYLPHENETHYL ALCOHOL is used as an intermediate in the synthesis of various drugs. Its aromatic nature and alcohol functionality make it a valuable component in the development of new medications with specific therapeutic properties.
Used in Fragrance Industry:
2-METHYLPHENETHYL ALCOHOL is used as a base material for the development of fragrances and perfumes. Its aromatic properties contribute to the creation of unique and complex scents, making it a valuable asset in the fragrance formulation process.
Used in Flavor Industry:
In the flavor industry, 2-METHYLPHENETHYL ALCOHOL is used to impart specific taste and aroma characteristics to food and beverages. Its unique chemical structure allows it to contribute to the overall flavor profile of various products, enhancing their sensory appeal.
Used in Research and Development:
2-METHYLPHENETHYL ALCOHOL is also used in research and development settings, where it serves as a model compound for studying various chemical reactions and processes. Its clear, colorless liquid form makes it an ideal candidate for experimental work and the development of new synthetic methodologies.
Synthesis Reference(s)
The Journal of Organic Chemistry, 22, p. 1202, 1957 DOI: 10.1021/jo01361a020
Flammability and Explosibility
Nonflammable
Check Digit Verification of cas no
The CAS Registry Mumber 19819-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,1 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19819-98:
(7*1)+(6*9)+(5*8)+(4*1)+(3*9)+(2*9)+(1*8)=158
158 % 10 = 8
So 19819-98-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O/c1-8-4-2-3-5-9(8)6-7-10/h2-5,10H,6-7H2,1H3
19819-98-8Relevant articles and documents
Lewis acid-promoted conjugate addition of functionalised organolithium compounds to electrophilic olefins
Yus, Miguel,Pastor, Isidro M,Gomis, Joaquín
, p. 5799 - 5805 (2001)
The reaction of several functionalised organolithium compounds 1-3 with different α,β-unsaturated ketones or esters 4-12 in the presence of a Lewis acid [ZnX2 (X=Cl, Br, I), AlCl3, FeCl3, BF3] leads, after hydrolysis, mainly to 1,4-addition products 13-31.
Exhaustive Reduction of Esters Enabled by Nickel Catalysis
Cook, Adam,Prakash, Sekar,Zheng, Yan-Long,Newman, Stephen G.
supporting information, p. 8109 - 8115 (2020/05/20)
We report a one-step procedure to directly reduce unactivated aryl esters into their corresponding tolyl derivatives. This is achieved by an organosilane-mediated ester hydrosilylation reaction and subsequent Ni/NHC-catalyzed hydrogenolysis. The resulting conditions provide a direct and efficient alternative to multi-step procedures for this transformation that often require the use of hazardous metal hydrides. Applications in the synthesis of -CD3-containing products, derivatization of bioactive molecules, and chemoselective reduction in the presence of other C-O bonds are demonstrated.
Pyrazine dicarboxylate-bridged arsenotungstate: Synthesis, characterization, and catalytic activities in epoxidation of olefins and oxidation of alcohols
Ma, Xinyi,He, Peipei,Xu, Baijie,Lu, Jingkun,Wan, Rong,Wu, Hechen,Wang, Yuan,Ma, Pengtao,Niu, Jingyang,Wang, Jingping
supporting information, p. 12956 - 12963 (2019/09/07)
A praseodymium(iii)-containing arsenotungstate K16H15Li7[Pr2(H2O)3(pzdc)As3W29O103]2·38H2O (1) (pzdc = pyrazine-2,3-dicarboxylic acid) was synthesized by a conventional aqueous solution method and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis (TGA), powder X-ray diffraction (PXRD), and single crystal X-ray diffraction. Structural analysis revealed that compound 1 was constructed by two identical subunits {Pr2(H2O)3(AsW9O33)3W2O4} bridged together by two pzdc ligands. In addition, compound 1 could act as an efficient catalyst for the epoxidation of olefins and oxidation of alcohols with hydrogen peroxide (H2O2) as the oxidant. In particular, the turnover frequency (TOF) in the oxidation of 1-phenylethanol reached up to 10170 h-1, which is higher than that of previously reported catalysts.
