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2(5H)-Furanone, 3-bromo-4-(phenylethynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

672304-81-3

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672304-81-3 Usage

Molecular Structure

The compound has a furanone ring, a bromine atom substituted at the 3 position, and a phenylethynyl group at the 4 position.

Molecular Weight

255.08 g/mol

Appearance

The compound is a pale yellow solid.

Solubility

It is soluble in common organic solvents such as ethanol, methanol, and acetone.

Biological Activity

Studies have shown that 2(5H)-Furanone, 3-bromo-4-(phenylethynyl)may have potential applications in the treatment of various diseases and disorders.

Reactivity

The compound's unique structure and reactivity make it an interesting target for chemical manipulation and drug development.

Research Interest

2(5H)-Furanone, 3-bromo-4-(phenylethynyl)is commonly used in organic synthesis and pharmaceutical research due to its potential biological activities and unique structure.

Check Digit Verification of cas no

The CAS Registry Mumber 672304-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,2,3,0 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 672304-81:
(8*6)+(7*7)+(6*2)+(5*3)+(4*0)+(3*4)+(2*8)+(1*1)=153
153 % 10 = 3
So 672304-81-3 is a valid CAS Registry Number.

672304-81-3Downstream Products

672304-81-3Relevant articles and documents

Regioselective synthesis of cytotoxic 4-(1-alkynyl)-substituted 2-(5H)-furanones

Bellina, Fabio,Falchi, Elisabetta,Rossi, Renzo

, p. 9091 - 9100 (2003)

4-(1-Alkynyl)-3-bromo- and 4-(1-alkynyl)-3-chloro-2(5H)-furanones have been regioselectively synthesized in moderate to good yields by a new version of the Pd/Cu-catalyzed Sonogashira reaction involving treatment of 1-alkynes with 3,4-dibromo- and 3,4-dic

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