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55994-35-9

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55994-35-9 Usage

Category

organic chemicals

Usage

organic synthesis, pharmaceutical research

Physical state

yellow solid at room temperature

Solubility

sparingly soluble in water

Main application

medicinal chemistry, potential pharmacological properties (requires further research for full understanding of its potential uses and effects)

Check Digit Verification of cas no

The CAS Registry Mumber 55994-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,9 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55994-35:
(7*5)+(6*5)+(5*9)+(4*9)+(3*4)+(2*3)+(1*5)=169
169 % 10 = 9
So 55994-35-9 is a valid CAS Registry Number.

55994-35-9Relevant articles and documents

A complete 1H and 13C NMR data assignment for 3-phenylmethylene-1H,3H-naphtho-[1,8-c,d]-pyran-1-one

Penchev, Plamen N.,Stoyanov, Neyko M.,Marinov, Marin N.

experimental part, p. 559 - 565 (2011/03/17)

Complete assignments of the 1H and 13C NMR chemical shifts for 3-phenylmethylene-1H,3H-naphtho-[1,8-c,d]-pyran-1-one were done by means of one- and two-dimensional NMR techniques, including 1H- 1H COSY, HMQC and

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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