Cas 1217079-06-5,ethyl (E)-7-(4-bromobenzylidene)-4-(4-bromophenyl)-6-oxospiro[4.4]non-1-ene-1-carboxylate

1217079-06-5

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Basic information

Product Name: ethyl (E)-7-(4-bromobenzylidene)-4-(4-bromophenyl)-6-oxospiro[4.4]non-1-ene-1-carboxylate
Synonyms: ethyl (E)-7-(4-bromobenzylidene)-4-(4-bromophenyl)-6-oxospiro[4.4]non-1-ene-1-carboxylate
CAS NO:1217079-06-5
Molecular Formula:
Molecular Weight: 530.256
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 (E)-7-(4-bromobenzylidene)-4-(4-bromophenyl)-6-oxospiro[4.4]non-1-ene-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (E)-7-(4-bromobenzylidene)-4-(4-bromophenyl)-6-oxospiro[4.4]non-1-ene-1-carboxylate(1217079-06-5)
EPA Substance Registry System: ethyl (E)-7-(4-bromobenzylidene)-4-(4-bromophenyl)-6-oxospiro[4.4]non-1-ene-1-carboxylate(1217079-06-5)

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: 1217079-06-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1217079-06-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,0,7 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1217079-06:
(9*1)+(8*2)+(7*1)+(6*7)+(5*0)+(4*7)+(3*9)+(2*0)+(1*6)=135
135 % 10 = 5
So 1217079-06-5 is a valid CAS Registry Number.

1217079-06-5Upstream product

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1217079-06-5Relevant academic research and scientific papers

Expanding the scope of Enantioselective FerroPHANE-promoted [3+2] annulations with α,β-unsaturated ketones

Pinto, Nathalie,Neel, Mathilde,Panossian, Armen,Retailleau, Pascal,Gilles Frison,Voituriez, Arnaud,Marinetti, Angela

experimental part, p. 1033 - 1045 (2010/05/19)

The planar chiral 2-phospha [3]ferrocenophane I has been shown to be the first efficient nucleo- philic organocatalyst for the enantiose- lective synthesis of cyclopentenyl- phosphonates, through [3+2] cycliza- tions between diethyl allenylphospho- nate a

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