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methyl 4-(2-fluorophenylamino)-2,5-dihydro-5-oxo-2-phenylfuran-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1372557-83-9

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1372557-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1372557-83-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,5,5 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1372557-83:
(9*1)+(8*3)+(7*7)+(6*2)+(5*5)+(4*5)+(3*7)+(2*8)+(1*3)=179
179 % 10 = 9
So 1372557-83-9 is a valid CAS Registry Number.

1372557-83-9Downstream Products

1372557-83-9Relevant articles and documents

Simple, convenient method for the synthesis of substituted furan-2(5 H)-one derivatives using tin(II) chloride

Nagarapu, Lingaiah,Kumar, U. Nikhil,Upendra,Bantu, Rajashaker

, p. 2139 - 2148 (2012)

Furan-2(5H)-one derivatives have been synthesized by a simple, efficient, one-pot, three-component condensation of anilines, dimethylacetylenedicarboxylate, and aromatic aldehydes in the presence of a catalytic amount of tin(II) chloride in excellent yields.

ZnO nanoparticle-catalyzed efficient one-pot three-component synthesis of 3,4,5-trisubstituted furan-2(5H)-ones

Tekale, Sunil U.,Kauthale, Sushma S.,Pagore, Vijay P.,Jadhav, Vivekanand B.,Pawar, Rajendra P.

, p. 1271 - 1277 (2013/11/06)

An efficient and high-yielding protocol using nano-ZnO (50-100 nm) as an efficient heterogeneous catalyst for one-pot three-component synthesis of pharmacologically significant furanone derivatives by the condensation of aromatic aldehyde, amine and dimethylacetylenedicarboxylate has been developed. Since the catalyst is heterogeneous, it can be easily separated and recycled several times without much loss of its catalytic activity. Use of aqueous medium, recyclable nanocatalyst, operational simplicity, non-chromatographic purification technique, excellent yield and short reaction time makes this approach an attractive protocol for the synthesis of 3,4,5-trisubstituted furan-2(5H)-ones.

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