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Naphtho[2,3-b]furan-2(3H)-one is an organic compound with the molecular formula C11H6O2. It is a heterocyclic aromatic compound, featuring a naphthalene ring fused to a furan ring, with a carbonyl group at the 2-position. Naphtho[2,3-b]furan-2(3H)-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be synthesized through various methods, including the condensation of 2-naphthol with aldehydes or ketones in the presence of an acid catalyst. The compound's properties, such as its solubility and stability, can be influenced by the presence of substituents on the naphthalene and furan rings. Naphtho[2,3-b]furan-2(3H)-one is an important intermediate in the preparation of more complex molecules, and its study contributes to the understanding of the chemistry of heterocyclic compounds.

4420-43-3

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4420-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4420-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4420-43:
(6*4)+(5*4)+(4*2)+(3*0)+(2*4)+(1*3)=63
63 % 10 = 3
So 4420-43-3 is a valid CAS Registry Number.

4420-43-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name naphtho[2,3-b]furan-2(3H)-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:4420-43-3 SDS

4420-43-3Downstream Products

4420-43-3Relevant academic research and scientific papers

Metal-free oxidative cyclization of alkynyl aryl ethers to benzofuranones

Graf, Katharina,Ruehl, Carmen L.,Rudolph, Matthias,Rominger, Frank,Hashmi, A. Stephen K.

, p. 12727 - 12731 (2013)

Readily available phenols can be converted into substituted aryl alkynyl ethers, which react with an N-oxide as an oxidant and catalytic amounts of a Bronsted acid to provide benzofuranones. If non-terminal alkynyl ethers are applied, a 1,2-hydride shift takes place and phenyl acrylates are obtained. Thus activated alkynes can serve as α-oxy carbene precursors even in the absence of a metal catalyst. Copyright

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