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α-Naphthal-γ-phenyl-crotonolactone is a complex organic compound characterized by its unique molecular structure, which features a naphthalene ring, a phenyl group, and a crotonolactone moiety. α-naphthal-γ-phenyl-crotonolactone is known for its potential applications in various chemical and pharmaceutical industries, particularly in the synthesis of certain drugs and other bioactive molecules. Its chemical properties, such as reactivity and stability, make it a valuable intermediate in organic synthesis. The compound's structure also contributes to its potential use in materials science, where it could be employed in the development of new polymers or other advanced materials. Overall, α-naphthal-γ-phenyl-crotonolactone represents an intriguing area of study within the field of organic chemistry, with potential implications for the creation of new compounds with diverse applications.

78013-98-6

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78013-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78013-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,1 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78013-98:
(7*7)+(6*8)+(5*0)+(4*1)+(3*3)+(2*9)+(1*8)=136
136 % 10 = 6
So 78013-98-6 is a valid CAS Registry Number.

78013-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-oxo-5-phenylfuran-3(2H)-ylidene)-1H,3H-benzo[de]isochromen-1-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

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More Details:78013-98-6 SDS

78013-98-6Relevant academic research and scientific papers

Reactions of Naphthalic Anhydride with β-Benzoylpropionic Acid and Hippuric Acid

El-Maghraby, M. A.,Koraiem, A. I. M.

, p. 73 - 74 (2007/10/02)

Naphthalic anhydride undergoes condensation with β-benzoylpropionic acid and hippuric acid to give α-naphthal-γ-phenyl-crotonolactone (I) and 4-naphthal-2-phenyl-5-oxazolone (II), respectively.Condensation of I and II with aldehydes gives the corresponding arylidenenaphthalides (V) while with hydrazine hydrate and benzylamine, aminonaphthalimide (III) and N,N'-dibenzylnaphthalamide (IV) respectively are formed.

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