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2-methyl-1-(4-chlorophenyl)-2,3-butadien-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138895-07-5

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138895-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138895-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,8,9 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138895-07:
(8*1)+(7*3)+(6*8)+(5*8)+(4*9)+(3*5)+(2*0)+(1*7)=175
175 % 10 = 5
So 138895-07-5 is a valid CAS Registry Number.

138895-07-5Relevant academic research and scientific papers

Experimental and theoretical studies of the propargyl-allenylindium system

Miao, Weishi,Chung, Lung Wa,Wu, Yun-Dong,Chan, Tak Hang

, p. 13326 - 13334 (2004)

The transient organoindium intermediates formed in the reaction of propargyl bromide with indium in aqueous media and tetrahydrofuran were investigated by NMR spectroscopy and found to be allenylindium(I) and allenylindium(III) dibromide. The influence of

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

Acid-catalyzed synthesis of α,β-disubstituted conjugated enones by a Meyer-Schuster-type rearrangement in allenols

Alcaide, Benito,Almendros, Pedro,Cembellín, Sara,Martínez Del Campo, Teresa

supporting information, p. 1070 - 1078 (2015/03/30)

A novel, direct and simple methodology to gain access to α,β-disubstituted conjugated enones from α-allenols in a sustainable metal catalysis context, considering the inexpensiveness and environmentally friendliness of iron(III) species and protons, has b

Carbonyl allenylations and propargylations by 3-chloro-1-propyne or 2-propynyl mesylates with tin(IV) chloride and tetrabutylammonium iodide

Masuyama, Yoshiro,Watabe, Akiko,Kurusu, Yasuhiko

, p. 1713 - 1715 (2007/10/03)

By the use of tin(IV) chloride and tetrabutylammonium iodide in dichloromethane, 3-chloro-1-propyne or 2-propynyl mesylate can be applied to allenylation and propargylation of aldehydes (carbonyl allenylation and propargylation) to produce a mixture of 1-

On pentaorganylstiborane. III. Regio- and diastereoselective additions of acetylenic and allenic organoantimony compounds to aldehydes

Zhang, Li-Jun,Mo, Xue-Sheng,Huang, Yao-Zeng

, p. 77 - 86 (2007/10/02)

The reaction of propargyl bromide (4a) with tributylstibine gave allenyltributylstibonium bromide (5), and its corresponding pentaorganylstiborane reacted with aldehyde to give homopropargylic alcohol (10a) exclusively in good yield.However, the reaction

Selective Synthesis of Allenic and Acetylenic Derivatives via Pentaorganylstiboranes

Zhang, Li-Jun,Huang, Yao-Zeng,Huang, Zhe-Hui

, p. 6579 - 6582 (2007/10/02)

Allenyltetrabutylstiborane (3), formed from allenyltributylstibonium bromide (2) and butylmagnesium bromide, reacted with aldehydes to give homopropargylic alcohols (4) exclusively in excellent yields, while 2-butynyltetrabutylstiborane (6), formed from 2

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