Cas 1207436-05-2,ethyl 5-oxo-3-phenyl-2-((1E,3E)-4-phenylbuta-1,3-dienyl)-2,5-dihydrofuran-2-carboxylate

1207436-05-2

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Basic information

Product Name: ethyl 5-oxo-3-phenyl-2-((1E,3E)-4-phenylbuta-1,3-dienyl)-2,5-dihydrofuran-2-carboxylate
Synonyms: ethyl 5-oxo-3-phenyl-2-((1E,3E)-4-phenylbuta-1,3-dienyl)-2,5-dihydrofuran-2-carboxylate
CAS NO:1207436-05-2
Molecular Formula:
Molecular Weight: 360.409
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 5-oxo-3-phenyl-2-((1E,3E)-4-phenylbuta-1,3-dienyl)-2,5-dihydrofuran-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 5-oxo-3-phenyl-2-((1E,3E)-4-phenylbuta-1,3-dienyl)-2,5-dihydrofuran-2-carboxylate(1207436-05-2)
EPA Substance Registry System: ethyl 5-oxo-3-phenyl-2-((1E,3E)-4-phenylbuta-1,3-dienyl)-2,5-dihydrofuran-2-carboxylate(1207436-05-2)

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: 1207436-05-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1207436-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,4,3 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1207436-05:
(9*1)+(8*2)+(7*0)+(6*7)+(5*4)+(4*3)+(3*6)+(2*0)+(1*5)=122
122 % 10 = 2
So 1207436-05-2 is a valid CAS Registry Number.

1207436-05-2Upstream product

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1207436-05-2Relevant academic research and scientific papers

N-heterocyclic carbene catalyzed transformations of 3-halopropenals to the equivalents of β-acylvinyl anions

Wu, Yihua,Yao, Weijun,Pan, Lianjie,Zhang, Yiping,Ma, Cheng

supporting information; experimental part, p. 640 - 643 (2010/05/18)

[Chemical equation presented] 3-Halopropenals 1 can behave as an alternative equivalent of β-acylvinyl anions (I) In the presence of N-heterocyclic carbene precursor (IPr-HCI) and DBU to afford cyclic αβ-unsaturated carbonyl derivatives, butenolides 4 and

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