Cas 1399075-96-7,ethyl 8-chloro-4-oxo-3-phenyl-3,4-dihydro-2H-furo[3,2-c]chromene-2-carboxylate

1399075-96-7

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Basic information

Product Name: ethyl 8-chloro-4-oxo-3-phenyl-3,4-dihydro-2H-furo[3,2-c]chromene-2-carboxylate
Synonyms: ethyl 8-chloro-4-oxo-3-phenyl-3,4-dihydro-2H-furo[3,2-c]chromene-2-carboxylate
CAS NO:1399075-96-7
Molecular Formula:
Molecular Weight: 370.789
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: ethyl 8-chloro-4-oxo-3-phenyl-3,4-dihydro-2H-furo[3,2-c]chromene-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 8-chloro-4-oxo-3-phenyl-3,4-dihydro-2H-furo[3,2-c]chromene-2-carboxylate(1399075-96-7)
EPA Substance Registry System: ethyl 8-chloro-4-oxo-3-phenyl-3,4-dihydro-2H-furo[3,2-c]chromene-2-carboxylate(1399075-96-7)

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: 1399075-96-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1399075-96-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,9,0,7 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1399075-96:
(9*1)+(8*3)+(7*9)+(6*9)+(5*0)+(4*7)+(3*5)+(2*9)+(1*6)=217
217 % 10 = 7
So 1399075-96-7 is a valid CAS Registry Number.

1399075-96-7Upstream product

1399075-96-7Downstream Products

1399075-96-7Relevant academic research and scientific papers

Water-compatible cascade reaction: An efficient route to substituted 2, 3-dihydrofurans

Zhang, Ya-Ru,Luo, Fang,Huang, Xu-Jiao,Xie, Jian-Wu

supporting information; experimental part, p. 777 - 779 (2012/09/07)

A highly efficient domino Michael additionalkylation reaction of 1, 3-dicarbonyl derivatives with 2-nitroacrylates was developed in water. The procedure tolerates a series of functional groups such as methoxy, bromo, chloro, and heteroaromatic groups, providing three types of 2, 3-dihydrofuran derivatives in moderate to good yields.

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