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(E)-3-(furan-2-yl)-1-phenylprop-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120134-60-3

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120134-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120134-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,3 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 120134-60:
(8*1)+(7*2)+(6*0)+(5*1)+(4*3)+(3*4)+(2*6)+(1*0)=63
63 % 10 = 3
So 120134-60-3 is a valid CAS Registry Number.

120134-60-3Relevant academic research and scientific papers

Transition-Metal-Free Synthesis of Homo- and Hetero-1,2,4-Triaryl Benzenes by an Unexpected Base-Promoted Dearylative Pathway

Rehan, Mohammad,Maity, Sanjay,Morya, Lalit Kumar,Pal, Kaushik,Ghorai, Prasanta

supporting information, p. 7728 - 7732 (2016/07/07)

An unprecedented approach for the synthesis of homo- and hetero-1,2,4-triaryl benzenes has been developed using a simple base-mediated reaction of either α-aryl cinnamyl alcohols or α,γ-di-aryl propanones. The salient feature of this strategy involves the sequential hydride transfer, regiospecific condensation, regiospecific dearylation, and aromatization under metal-free reaction conditions. The synthesis of unsymmetrically substituted triphenylenes by oxidative coupling of the synthesized 1,2,4-triaryl benzenes has also been demonstrated.

Convergent synthesis of conjugated 1,2-disubstituted E-allylic alcohols from two aldehydes and methylenetriphenylphosphorane

Hodgson, David M.,Persaud, Rosanne S. D.

supporting information, p. 7949 - 7951 (2013/06/27)

β-Lithiooxyphosphonium ylides, made in situ from an aldehyde and methylenetriphenylphosphorane, react with a second aldehyde to form E-allylic alcohols. α-Branching and α,β-unsaturation in the second aldehyde, together with the lack of further substitution on the phosphorane carbon play important roles in selectivity. A range of these aldehydes, in addition to aromatic aldehydes as the second aldehyde also provided synthetically useful access to E-allylic alcohols.

Reduction of activated conjugated alkenes by the InCl3-NaBH 4 reagent system

Ranu, Brindaban C.,Samanta, Sampak

, p. 7901 - 7906 (2007/10/03)

A combination of a catalytic amount of indium (III) chloride and sodium borohydride in acetonitrile reduces selectively the carbon-carbon double bonds in conjugated alkenes such as α,α-dicyano olefins, α,β-unsaturated nitriles, cyanoesters, cyanophosphonate and dicarboxylic esters. However, reduction of chalcones is little different. They are reduced to a mixture of saturated ketones and alcohols if the reaction mixture is quenched with H2O, whereas quenching with MeOH leads to saturated alcohols only.

CYCLOPENTENONE DERIVATIVES BY SOLVOLYSIS OF 2-FURYLIDENE CARBINOLS

Antonioletti, Roberto,Mico, Antonella De,Piancatelli, Giovanni,Scettri, Arrigo,Ursini, Ornella

, p. 745 - 746 (2007/10/02)

Solvolytic treatment of 2-furylidene carbinols 1 leads to cyclopentenones 2 in satisfactory yields only under carefully chosen experimental conditions.Otherwise, a very interesting competitive process, implying the conversion of 1 into a quite different c

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