Cas 1607832-30-3,(E)-ethyl 3-oxo-2-(2-oxoacenaphthylen-1(2H)-ylidene)-3-phenylpropanoate

1607832-30-3

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Basic information

Product Name: (E)-ethyl 3-oxo-2-(2-oxoacenaphthylen-1(2H)-ylidene)-3-phenylpropanoate
Synonyms: (E)-ethyl 3-oxo-2-(2-oxoacenaphthylen-1(2H)-ylidene)-3-phenylpropanoate
CAS NO:1607832-30-3
Molecular Formula:
Molecular Weight: 356.378
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (E)-ethyl 3-oxo-2-(2-oxoacenaphthylen-1(2H)-ylidene)-3-phenylpropanoate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-ethyl 3-oxo-2-(2-oxoacenaphthylen-1(2H)-ylidene)-3-phenylpropanoate(1607832-30-3)
EPA Substance Registry System: (E)-ethyl 3-oxo-2-(2-oxoacenaphthylen-1(2H)-ylidene)-3-phenylpropanoate(1607832-30-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1607832-30-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1607832-30-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,7,8,3 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1607832-30:
(9*1)+(8*6)+(7*0)+(6*7)+(5*8)+(4*3)+(3*2)+(2*3)+(1*0)=163
163 % 10 = 3
So 1607832-30-3 is a valid CAS Registry Number.

1607832-30-3Upstream product

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1607832-30-3Relevant academic research and scientific papers

Direct β-acylation of 2-arylidene-1,3-indandiones with acyl chlorides catalyzed by organophosphanes

Lee, Chia-Jui,Sheu, Chia-Ning,Tsai, Cheng-Che,Wu, Zong-Ze,Lin, Wenwei

, p. 5304 - 5306 (2014)

We have developed an organophosphane-catalyzed direct β-acylation of a series of conjugated systems bearing ketone, amide and ester functionalities using acyl chlorides as trapping reagents. A wide variety of highly functional ketone derivatives were gene

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