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ethyl 5-(4-methoxyphenyl)-2-methyl-4,5-dihydrofuran-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74947-72-1

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74947-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74947-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,4 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74947-72:
(7*7)+(6*4)+(5*9)+(4*4)+(3*7)+(2*7)+(1*2)=171
171 % 10 = 1
So 74947-72-1 is a valid CAS Registry Number.

74947-72-1Downstream Products

74947-72-1Relevant academic research and scientific papers

Evidence of CuI/CuII Redox Process by X-ray Absorption and EPR Spectroscopy: Direct Synthesis of Dihydrofurans from β-Ketocarbonyl Derivatives and Olefins

Yi, Hong,Liao, Zhixiong,Zhang, Guanghui,Zhang, Guoting,Fan, Chao,Zhang, Xu,Bunel, Emilio E.,Pao, Chih-Wen,Lee, Jyh-Fu,Lei, Aiwen

, p. 18925 - 18929 (2015)

The CuI/CuII and CuI/CuIII catalytic cycles have been subject to intense debate in the field of copper-catalyzed oxidative coupling reactions. A mechanistic study on the CuI/CuII redox proc

Organocatalytic Cloke-Wilson Rearrangement: DABCO-Catalyzed Ring Expansion of Cyclopropyl Ketones to 2,3-Dihydrofurans

Zhang, Jingfang,Tang, Yuhai,Wei, Wen,Wu, Yong,Li, Yang,Zhang, Junjie,Zheng, Yuansuo,Xu, Silong

, p. 3043 - 3046 (2017/06/23)

An organocatalytic Cloke-Wilson rearrangement of cyclopropyl ketones to 2,3-dihydrofurans is exploited utilizing the homoconjugate addition process. With 1,4-diazabicyclo[2.2.2]octane as the catalyst, the rearrangement in DMSO at 120 °C proceeded in gener

Aluminium Oxide Assisted Stereoselective Rearrangement of a Cyclopropyl Ketone to 4,5-Dihydrofuran

Alonso, Miguel E.,Morales, Angelina

, p. 4530 - 4532 (2007/10/02)

Contrary to the general observation that thermally and photochemically induced cyclopropyl ketone to dihydrofuran arrangements take place with partial loss of the stereochemical identity of the starting cyclopropane, a characteristic shared by the closely related vinylcyclopropanes and vinyloxiranes, a case of totally stereospecific, alumina-assisted cyclopropyl ketone to dihydrofuran rearrangement at room temperature was observed.

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