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(1-Methoxy-2-methyl-buta-2,3-dienyl)-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72014-31-4

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72014-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72014-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,1 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72014-31:
(7*7)+(6*2)+(5*0)+(4*1)+(3*4)+(2*3)+(1*1)=84
84 % 10 = 4
So 72014-31-4 is a valid CAS Registry Number.

72014-31-4Downstream Products

72014-31-4Relevant academic research and scientific papers

ACTION D'ALUMINIQUES DERIVANT DE BROMURES RCCCH2Br SUR LES ACETALS; PREPARATION D'ETHERS α-ALLENIQUES

Barbot, F.,Miginiac, Ph.

, p. 83 - 86 (1986)

Organoaluminium compounds prepared in ether from RCCCH2Br react with acetals to give solely α-allenic ethers.

Organoseleno-catalyzed synthesis of α,β-unsaturated α′-Alkoxy ketones from allenes enabled by se···o interactions

Toledano-Pinedo, Mireia,Martínez Del Campo, Teresa,Tiemblo, Marta,Fernández, Israel,Almendros, Pedro

supporting information, p. 3979 - 3984 (2020/05/14)

α,β-Unsaturated α′-Alkoxy ketones have been prepared under mild conditions from allenes using water as the oxygen source and without the necessity of metals. The organocatalytic oxygenation-rearrangement sequence displays an exquisite chemo-, stereo-, and

Lewis acid-catalyzed three-component condensation reactions of aldehydes, alkoxysilanes, and propargylsilane: Synthesis of α-allenyl ethers

Niimi, Lui,Shiino, Keitaro,Hiraoka, Shuichi,Yokozawa, Tsutomu

, p. 1721 - 1724 (2007/10/03)

For simultaneous construction of a polyether backbone and the allenyl side chains, Lewis acid-catalyzed three-component condensation reactions of aldehydes, alkoxytrimethylsilanes, and 1-trimethylsilyl-2-butyne were studied. The reaction of these three compounds took place in the presence of a catalytic amount of TrClO4 at -78°C to yield the corresponding α-allenyl ethers in good yields. This reaction was also applied to the synthesis of a polyether having allenyl side chains.

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