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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.

19819-98-8

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19819-98-8 Usage

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

19819-98-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylphenyl)ethanol

1.2 Other means of identification

Product number -
Other names 2-(o-methylphenyl)-ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19819-98-8 SDS

19819-98-8Relevant academic research and scientific papers

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.

Epoxide Electroreduction

Huang, Cheng,Lu, Qingquan,Ma, Wan,Qi, Xiaotian,Xu, Minghao,Zheng, Xuelian

supporting information, p. 1389 - 1395 (2022/01/19)

Selective hydrogenation of epoxides would be a direct and powerful approach for alcohol synthesis, but it has proven to be elusive. Here, electrochemically epoxide hydrogenation using electrons and protons as reductants is reported. A wide range of primary, secondary, and tertiary alcohols can be achieved through selective Markovnikov or anti-Markovnikov ring opening in the absence of transition metals. Mechanistic investigations revealed that the regioselectivity is controlled by the thermodynamic stabilities of the in situ generated benzyl radicals for aryl-substituted epoxides and the kinetic tendency for Markovnikov selective ring opening for alkyl-substituted epoxides.

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.

Iron-Catalyzed β-Alkylation of Alcohols

Bettoni, Leó,Gaillard, Sylvain,Renaud, Jean-Luc

supporting information, p. 8404 - 8408 (2019/10/16)

β-Branched alkylated alcohols have been prepared in good yields using a double-hydrogen autotransfer strategy in the presence of our diaminocyclopentadienone iron tricarbonyl complex Fe1. The alkylation of some 2-arylethanol derivatives was successfully addressed with benzylic alcohols and methanol as alkylating reagents under mild conditions. Deuterium labeling experiments suggested that both alcohols (2-arylethanol and either methanol or benzyl alcohol) served as hydrogen donors in this cascade process.

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.

Visible-Light-Mediated Aerobic Oxidation of Organoboron Compounds Using in Situ Generated Hydrogen Peroxide

Weng, Wei-Zhi,Liang, Hao,Zhang, Bo

, p. 4979 - 4983 (2018/08/24)

A simple and general visible-light-mediated oxidation of organoboron compounds has been developed with rose bengal as the photocatalyst, substoichiometric Et3N as the electron donor, as well as air as the oxidant. This mild and metal-free protocol shows a broad substrate scope and provides a wide range of aliphatic alcohols and phenols in moderate to excellent yields. Notably, the robustness of this method is demonstrated on the stereospecific aerobic oxidation of organoboron compounds.

Photochemical Homologation for the Preparation of Aliphatic Aldehydes in Flow

Chen, Yiding,Leonardi, Marco,Dingwall, Paul,Labes, Ricardo,Pasau, Patrick,Blakemore, David C.,Ley, Steven V.

, p. 15558 - 15568 (2019/01/04)

Cheap and readily available aqueous formaldehyde was used as a formylating reagent in a homologation reaction with nonstabilized diazo compounds, enabled by UV photolysis of bench-stable oxadiazolines in a flow photoreactor. Various aliphatic aldehydes were synthesized along with the corresponding derivatized alcohols and benzimidazoles. No transition-metal catalyst or additive was required to affect the reaction, which proceeded at room temperature in 80 min.

TiO2-Supported Re as a General and Chemoselective Heterogeneous Catalyst for Hydrogenation of Carboxylic Acids to Alcohols

Toyao, Takashi,Siddiki, S. M. A. Hakim,Touchy, Abeda S.,Onodera, Wataru,Kon, Kenichi,Morita, Yoshitsugu,Kamachi, Takashi,Yoshizawa, Kazunari,Shimizu, Ken-Ichi

, p. 1001 - 1006 (2017/02/05)

TiO2-supported Re, Re/TiO2, was found to promote selective hydrogenation of carboxylic acids having aromatic and aliphatic moieties to the corresponding alcohols. Re/TiO2showed superior results compared to other transition-metal-loaded TiO2and supported Re catalysts for selective hydrogenation of 3-phenylpropionic acid. 3-phenylpropanol was produced in 97 % yield under mild conditions (5 MPa H2at 140 °C). Contrary to typical heterogeneous catalysts, Re/TiO2does not lead to the formation of dearomatized byproducts. The catalyst is recyclable and shows a wide substrate scope in the synthesis of alcohols (22 examples; up to 97 % isolated yield).

COMPOUNDS FROM RENEWABLE RESOURCES

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Paragraph 0326-0328, (2017/10/26)

Compounds of formula III: and salts thereof are disclosed. Also disclosed are methods for preparing compounds of formula III, intermediates useful for preparing compounds of formula III and methods for preparing compounds and materials from compounds of formula III.

Antiproliferative activity and SARs of caffeic acid esters with mono-substituted phenylethanols moiety

Xie, Jin,Yang, Fengzhi,Zhang, Man,Lam, Celine,Qiao, Yixue,Xiao, Jia,Zhang, Dongdong,Ge, Yuxuan,Fu, Lei,Xie, Dongsheng

, p. 131 - 134 (2016/12/27)

A series of CAPE derivatives with mono-substituted phenylethanols moiety were synthesized and evaluated by MTT assay on growth of 4 human cancer cell lines (Hela, DU-145, MCF-7 and ECA-109). The substituent effects on the antiproliferative activity were systematically investigated for the first time. It was found that electron-donating and hydrophobic substituents at 2′-position of phenylethanol moiety could significantly enhance CAPE's antiproliferative activity. 2′-Propoxyl derivative, as a novel caffeic acid ester, exhibited exquisite potency (IC50?=?0.4?±?0.02 & 0.6?±?0.03?μM against Hela and DU-145 respectively).

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