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Phenanthro[9,10-c]furan-1,3-dione is a chemical compound with the molecular formula C15H6O3. It is a derivative of phenanthrofuran, which is a heterocyclic compound consisting of a phenanthrene ring fused to a furan ring. This particular compound is characterized by the presence of two carbonyl groups (C=O) at the 1 and 3 positions of the furan ring. Phenanthro[9,10-c]furan-1,3-dione is known for its unique chemical structure and potential applications in various fields, such as organic synthesis and materials science. Its properties, reactivity, and potential uses are of interest to researchers in the field of chemistry, particularly those studying the synthesis and applications of heterocyclic compounds.

2510-53-4

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2510-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2510-53-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2510-53:
(6*2)+(5*5)+(4*1)+(3*0)+(2*5)+(1*3)=54
54 % 10 = 4
So 2510-53-4 is a valid CAS Registry Number.

2510-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name phenanthro[9,10-c]furan-1,3-dione

1.2 Other means of identification

Product number -
Other names 9,10-phenanthrenedicarboxylic anhydride

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2510-53-4 SDS

2510-53-4Relevant academic research and scientific papers

Ring Transformation of 3,4-Diphenyl-2-furylcarbamoyl Compounds to N-Substituted 3,4-Diphenyl-5-hydroxy-3-pyrrolin-2-ones

Yakushijin, Kenichi,Kozuka, Masamichi,Furukawa, Hiroshi

, p. 2178 - 2184 (2007/10/02)

3,4-Diphenyl-2-furylcarbamoyls (IIIa - e) react with oxygen in benzene at room temperature and in the abscence of catalysts or bases to give 3,4-diphenyl-5-hydroxy-3-pyrrolin-2-ones (Va - e) as main products.Under the same conditions, treatment of 3,4-diphenyl-2-furyl isocyanate (II) with an excess of various amines resulted in a clean autoxidation reaction to give Ve - h and diphenylmaleimides (XIIa - d) in a ratio of about 1:1. 3-Hydroxyphenantropyrrolin-1-ones (XIIIa - e) were prepared by the photocyclization of Va - e.

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