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(4-methoxyphenyl)(5-methylfuran-2-yl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

356552-15-3

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356552-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 356552-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,5,5 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 356552-15:
(8*3)+(7*5)+(6*6)+(5*5)+(4*5)+(3*2)+(2*1)+(1*5)=153
153 % 10 = 3
So 356552-15-3 is a valid CAS Registry Number.

356552-15-3Relevant academic research and scientific papers

Catalytic Formal Benzylic C-H Bond Functionalization of 2,5-Dialkylfuran Derivatives with Ferrocenyl Alcohols as Alkylation Reagents

Ren, Didi,Xu, Lubin,Wang, Liang,Li, Shuai-Shuai

supporting information, p. 627 - 631 (2019/02/12)

The inert benzylic C-H bond of π-electron-rich heteroaromatic 2,5-dialkylfuran derivatives was conveniently functionalized with ferrocenyl alcohols as alkylation reagents under catalytic acidic conditions at room temperature, which features chemo- and reg

Cobalt-Catalyzed Oxygenation/Dearomatization of Furans

Oswald, Jonathan P.,Woerpel

, p. 9067 - 9075 (2018/05/29)

The dearomatization of aromatic compounds using cobalt(II) acetylacetonate with triplet oxygen and triethylsilane converts furans, benzofurans, pyrroles, and thiophenes to a variety of products, including lactones, silyl peroxides, and ketones.

Gold catalysis: Non-spirocyclic intermediates in the conversion of furanynes by the formal insertion of an alkyne into an aryl-alkyl C-C single bond

Hashmi, A. Stephen K.,Haeffner, Tobias,Yang, Weibo,Pankajakshan, Sreekumar,Schaefer, Sascha,Schultes, Lara,Rominger, Frank,Frey, Wolfgang

supporting information, p. 10480 - 10486 (2012/11/07)

It takes al-kynes: The formation of furyl-substituted heterocycles from furanynes with donor groups on the furan-alkyne tether and mechanistic control experiments indicate the involvement of open-chained carbenium ions in the overall insertion of an alkyne into a C-C bond, rather than the usual spirocyclic intermediates (see scheme). Copyright

An easy access to unsymmetric trisubstituted methane derivatives (TRSMs)

Kumar Das, Sajal,Shagufta,Panda, Gautam

, p. 3097 - 3102 (2007/10/03)

A new series of unsymmetric trisubstituted methane derivatives (TRSMs) has been synthesized through Friedel-Crafts alkylation of aromatic nucleophiles using acid-sensitive heteroaryl carbinols.

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