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Benzenemethanol, 3-methoxy-α-2-propynyl-, also known as 3-methoxy-2-propynylbenzenemethanol or 3-methoxy-2-propynylbenzyl alcohol, is an organic compound with the chemical formula C10H12O2. It is a derivative of benzyl alcohol, featuring a 2-propynyl (propargyl) group and a methoxy group attached to the benzene ring. Benzenemethanol, 3-methoxy-a-2-propynyl- is characterized by its unique structure, which combines the properties of benzyl alcohol, propargyl, and methoxy groups. It is used in various applications, such as in the synthesis of pharmaceuticals, fragrances, and other organic compounds. Due to its versatile chemical structure, it can participate in a range of reactions, including substitution, addition, and condensation reactions, making it a valuable intermediate in organic chemistry.

42250-04-4

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42250-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42250-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,5 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42250-04:
(7*4)+(6*2)+(5*2)+(4*5)+(3*0)+(2*0)+(1*4)=74
74 % 10 = 4
So 42250-04-4 is a valid CAS Registry Number.

42250-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-methoxyphenyl)but-3-yn-1-ol

1.2 Other means of identification

Product number -
Other names 1-(m-methoxyphenyl)but-3-yn-1-ol

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:42250-04-4 SDS

42250-04-4Relevant academic research and scientific papers

Silylcyclopropanes by Selective [1,4]-Wittig Rearrangement of 4-Silyl-5,6-dihydropyrans

Mori-Quiroz, Luis M.,Maloba, Emmanuel W.,Maleczka, Robert E.

supporting information, p. 5724 - 5728 (2021/07/31)

4-Silyl-5,6-dihydropyrans undergo remarkably selective [1,4]-Wittig rearrangements to give silylcyclopropanes in good yields. The selectivity is independent of the silyl group, but it is influenced by the electronic character of the migrating center. Elec

Photoredox propargylation of aldehydes catalytic in titanium

Calogero, Francesco,Gualandi, Andrea,Di Matteo, Marco,Potenti, Simone,Fermi, Andrea,Bergamini, Giacomo,Cozzi, Pier Giorgio

, p. 7002 - 7009 (2021/05/29)

A practical and effective photoredox propargylation of aldehydes promoted by 10 mol % of [Cp2TiCl2] is presented. No stoichiometric metals or scavengers are used for the process. A catalytic amount of the cheap and simply prepared or

One-Pot γ-Lactonization of Homopropargyl Alcohols via Intramolecular Ketene Trapping

Yamane, Daichi,Tanaka, Haruna,Hirata, Akihiro,Tamura, Yumiko,Takahashi, Daichi,Takahashi, Yusuke,Nagamitsu, Tohru,Ohtawa, Masaki

supporting information, p. 2831 - 2835 (2021/05/05)

A one-pot γ-lactonization of homopropargyl alcohols via an alkyne deprotonation/boronation/oxidation sequence has been developed. Oxidation of the generated alkynyl boronate affords the corresponding ketene intermediate, which is trapped by the adjacent hydroxy group to furnish the γ-lactone. We have optimized the conditions as well as examined the substrate scope and synthetic applications of this efficient one-pot lactonization.

Gold-Catalyzed Tandem Oxidative Coupling Reaction between β-Ketoallenes and Electron-Rich Arenes to 2-Furylmethylarenes

Yasukawa, Naoki,Yamada, Yutaro,Furugen, Chikara,Miki, Yuya,Sajiki, Hironao,Sawama, Yoshinari

supporting information, p. 5891 - 5895 (2021/08/18)

A tandem oxidative coupling reaction of β-ketoallenes and arenes was developed, which leads to the formation of 2-furylmethylarenes using AuCl3 and phenyliodine diacetate. The AuIII salt catalyzed the cyclization of β-ketoallenes to form a 2-furylmethyl gold intermediate, and the subsequent C-H functionalization of arenes proceeded smoothly. During the oxidative coupling, nucleophilic additions occurred at the center and terminal carbon atoms of the allene moiety to form C-O and C-C bonds.

Efficient method for propargylation of aldehydes promoted by allenylboron compounds under microwave irradiation

Andrade, Silvia R. C. P.,Freitas, Jucleiton J. R.,Freitas, Juliano C. R.,Freitas, Queila P. S. B.,Menezes, Paulo H.,Oliveira, Roberta A.

supporting information, p. 168 - 174 (2020/03/27)

The propargylation of aldehydes promoted by microwave irradiation using allenylboron compounds in a chemo- and regioselective way is described. The corresponding products were obtained in short reaction time, high yield and purity without the need of any solvent when allenylboronic acid pinacol ester was used, or using a minimal amount of acetone when potassium allenyltrifluoroborate was used.

One-pot, regioselective synthesis of homopropargyl alcohols using pro-pargyl bromide and carbonyl compound by the mg-mediated reaction under solvent-free conditions

Devaramani, Samrat,Li, Shunxi,Ma, Xiaofang,Xu, Daqian,Zhao, Guohu

supporting information, p. 438 - 442 (2020/04/21)

The elimination of volatile organic solvents in organic synthesis is the most important goal in “Green” chemistry. We report a simple, efficient and facile method for the addition of progargyl bromide to carbonyl compounds using Mg metal as a mediator under solvent-free conditions which could regioselectively generate homopropargyl alcohols efficiently in good to excellent yields. The procedure has advantages such as short reaction time, operationally simple, excellent product yields, high regioselectivity and organic solvent-free.

Synthesis and characterization of nano?zinc wire using a self designed unit galvanic cell in aqueous medium and its reactivity in propargylation of aldehydes

Mondal, Bibhas,Mandal, Siba Prasad,Kundu, Mousumi,Adhikari,Roy, Ujjal Kanti

supporting information, p. 4669 - 4675 (2019/07/22)

Electrochemistry is used for propargylation of carbonyls in aqueous ZnCl2 medium. For electrochemical process we designed a unit galvanic cell. ZnCl2 is used as stoichiometric reagent and causes electrochemical deposition of zinc in

Scalable Regioselective and Stereoselective Synthesis of Functionalized (E)-4-Iodobut-3-en-1-ols: Gram-Scale Total Synthesis of Fungal Decanolides and Derivatives

Sherwood, Alexander M.,Williamson, Samuel E.,Johnson, Stephanie N.,Yilmaz, Anil,Day, Victor W.,Prisinzano, Thomas E.

, p. 980 - 992 (2018/01/27)

A reliable protocol to synthesize both racemic and chiral (E)-4-iodobut-3-en-1-ols from aldehydes or epoxides, respectively, containing various aromatic and aliphatic substitutions has been established. The utility of these compounds was then demonstrated

Atom-Economical Palladium Carbon-Catalyzed de Novo Synthesis of Trisubstituted Nicotinonitriles

Sarkar, Debayan,Rout, Nilendri,Ghosh, Manoj Kumar,Giri, Santanab,Neue, Kornelius,Reuter, Hans

, p. 9012 - 9022 (2017/09/11)

A de novo palladium carbon-catalyzed synthesis of trisubstituted nicotinonitriles from easily synthesized homopropagylic or homoallylic aromatic alcohols in the presence of nitriles has been explored. The mechanism proceeds with an interesting generation

C-Propargylation Overrides O-Propargylation in Reactions of Propargyl Chloride with Primary Alcohols: Rhodium-Catalyzed Transfer Hydrogenation

Liang, Tao,Woo, Sang Kook,Krische, Michael J.

supporting information, p. 9207 - 9211 (2016/08/05)

The canonical SN2 behavior displayed by alcohols and activated alkyl halides in basic media (O-alkylation) is superseded by a pathway leading to carbinol C-alkylation under the conditions of rhodium-catalyzed transfer hydrogenation. Racemic and asymmetric propargylations are described.

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