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Benzenemethanol, α-methyl-α-1-propynyl-, also known as 1-(4-hydroxybenzyl)-2-methyl-2-propyn-1-ol or 4-(2-methyl-3-butyn-2-yl)benzenemethanol, is an organic compound with the chemical formula C11H12O. It is a derivative of benzyl alcohol, featuring a propargyl group (3-butyn-2-yl) attached to the α-carbon of the benzyl alcohol moiety. Benzenemethanol, a-methyl-a-1-propynyl- is characterized by its unique structure, which combines the aromaticity of the benzene ring with the reactivity of the propargyl group, making it a potentially useful intermediate in the synthesis of various organic compounds and pharmaceuticals. Its molecular weight is 156.21 g/mol, and it is likely to exhibit properties such as low solubility in water and high solubility in organic solvents, due to its nonpolar nature.

6712-32-9

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6712-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6712-32-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6712-32:
(6*6)+(5*7)+(4*1)+(3*2)+(2*3)+(1*2)=89
89 % 10 = 9
So 6712-32-9 is a valid CAS Registry Number.

6712-32-9Relevant academic research and scientific papers

Alcohol Dehydrogenases and N-Heterocyclic Carbene Gold(I) Catalysts: Design of a Chemoenzymatic Cascade towards Optically Active β,β-Disubstituted Allylic Alcohols

González-Granda, Sergio,Lavandera, Iván,Gotor-Fernández, Vicente

supporting information, p. 13945 - 13951 (2021/04/22)

The combination of gold(I) and enzyme catalysis is used in a two-step approach, including Meyer–Schuster rearrangement of a series of readily available propargylic alcohols followed by stereoselective bioreduction of the corresponding allylic ketone intermediates, to provide optically pure β,β-disubstituted allylic alcohols. This cascade involves a gold N-heterocyclic carbene and an enzyme, demonstrating the compatibility of both catalyst types in aqueous medium under mild reaction conditions. The combination of [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene][bis(trifluoromethanesulfonyl)-imide]gold(I) (IPrAuNTf2) and a selective alcohol dehydrogenase (ADH-A from Rhodococcus ruber, KRED-P1-A12 or KRED-P3-G09) led to the synthesis of a series of optically active (E)-4-arylpent-3-en-2-ols in good yields (65–86 %). The approach was also extended to various 2-hetarylpent-3-yn-2-ol, hexynol, and butynol derivatives. The use of alcohol dehydrogenases of opposite selectivity led to the production of both allyl alcohol enantiomers (93->99 % ee) for a broad panel of substrates.

A Domino Strategy for the Synthesis of 2H-Pyrans from Propargyl Vinyl Ethers

Tejedor, David,Delgado-Hernández, Samuel,Diana-Rivero, Raquel,Díaz-Díaz, Abián,García-Tellado, Fernando

, p. 1784 - 1790 (2019/02/19)

Stable monocyclic 2H-pyrans are synthesized from readily available tertiary propargyl vinyl ethers via a metal-free all-pericyclic domino manifold involving a sequential propargyl Claisen rearrangement/[1,3]H-shift/oxa-6π electrocyclization set of reactions. The wide scope of this protocol is exemplified by the synthesis of 21 different 2H-pyrans incorporating a varied substitution pattern at the ring.

Gold-catalyzed isomerization of unactivated allenes into 1,3-dienes under ambient conditions

Ting, Chun-Ming,Hsu, Yi-Ling,Liu, Rai-Shung

supporting information; experimental part, p. 6577 - 6579 (2012/07/31)

We have developed a gold-catalyzed isomerization of unactivated allenes into 1,3-dienes with nitrosobenzene as an additive. This reaction proceeded almost exclusively at room temperature for highly substituted allenes. The utility of this reaction is manifested by the development of one-pot [4+2]-cycloaddition of allenes and reactive alkenes.

Using nazarov electrocyclization to stage chemoselective [1,2]-migrations: Stereoselective synthesis of functionalized cyclopentenones

Lebuf, David,Huang, Jie,Gandon, Vincent,Frontier, Alison J.

supporting information; experimental part, p. 10981 - 10985 (2011/12/16)

Highly functionalized cyclopentenones have been prepared stereospecifically through a chemoselective copper(II)-mediated Nazarov/Wagner-Meerwein rearrangement sequence. After the initial 4π electrocyclization, this reaction involves two sequential [1,2]-m

One-pot synthesis of optically active allyl esters via lipase-vanadium combo catalysis

Akai, Shuji,Hanada, Ryosuke,Fujiwara, Noboru,Kita, Yasuyuki,Egi, Masahiro

supporting information; experimental part, p. 4900 - 4903 (2011/01/12)

The combination of vanadium-oxo compounds (3 or 4) with a lipase produced the regio- and enantioconvergent transformation of racemic allyl alcohols (1 or 2) into optically active allyl esters. In this system, the vanadium compounds catalyzed the continuous racemization of the alcohols along with the transposition of the hydroxyl group, while the lipase effected the chemo- and enantioselective esterification to achieve the dynamic kinetic resolution.

Convenient generation of 1-propynyllithium. One-pot synthesis of acetylenic carbinols from 1,2-dibromopropane and aldehydes and ketones

Gribble,Joyner,Switzer

, p. 2997 - 3002 (2007/10/02)

Treatment of 1,2-dibromopropane (1) with 3 equiv of lithium diisopropylamide (-60° to 0°C, THF) generates 1-propynyllithium (2), which with aldehydes or ketones affords acetylenic carbinols 3 in 82-96% yields.

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