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2(3H)-Furanone, dihydro-5-[(3,4,5-trimethoxyphenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

848653-55-4

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848653-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848653-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,6,5 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 848653-55:
(8*8)+(7*4)+(6*8)+(5*6)+(4*5)+(3*3)+(2*5)+(1*5)=214
214 % 10 = 4
So 848653-55-4 is a valid CAS Registry Number.

848653-55-4Downstream Products

848653-55-4Relevant academic research and scientific papers

Chemo-, regio- and stereoselective heck arylation of allylated malonates: Mechanistic insights by ESI-MS and synthetic application toward 5-arylmethyl-γ-lactones

Oliveira, Caio C.,Marques, Marcelo V.,Godoi, Marla N.,Regiani, Thas,Santos, Vanessa G.,Santos, Emerson A.F. Dos,Eberlin, Marcos N.,S, Marcus M.,Correia, Carlos R.D.

, p. 5180 - 5183 (2014/12/11)

We describe herein a general method for the controlled Heck arylation of allylated malonates. Both electron-rich and electron-poor aryldiazonium salts were readily employed as the aryl-transfer agents in good yields and in high chemo-, regio-, and stereoselectivity without formation of decarboxylated byproducts. Reaction monitoring via ESI-MS was used to support the formation of chelated Pd species through the catalytic cycle. Additionally, some Heck adducts were successfully used in the total synthesis of pharmacologically active γ-lactones.

Synthesis and biological activity of the tea catechin metabolites, M4 and M6 and their methoxy-derivatives

Lambert, Joshua D.,Rice, Joseph E.,Hong, Jungil,Hou, Zhe,Yang, Chung S.

, p. 873 - 876 (2007/10/03)

Syntheses are reported for metabolites M4 (1) and M6 (2) of the green tea polyphenols epicatechin (EC) and epigallocatechin (EGC) and their gallate derivatives. Several methoxy-derivatives of 1 and 2 were also prepared. Compounds 1 and 2 were evaluated for growth inhibitory activity against a panel of immortalized and malignant human cell lines with 1 being the more active compound. The possible antiinflammatory activity of 1 and its trimethoxy derivative was also evaluated. Neither compound inhibited the release of arachidonic acid, although 1 inhibited NO production by 50% at 20 μM.

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