Cas 960505-59-3,(E)-1-(3-phenylprop-2-enoyl)naphthalen-2-yl nonafluorobutanesulfonate

960505-59-3

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Basic information

Product Name: (E)-1-(3-phenylprop-2-enoyl)naphthalen-2-yl nonafluorobutanesulfonate
Synonyms: (E)-1-(3-phenylprop-2-enoyl)naphthalen-2-yl nonafluorobutanesulfonate
CAS NO:960505-59-3
Molecular Formula:
Molecular Weight: 556.405
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)-1-(3-phenylprop-2-enoyl)naphthalen-2-yl nonafluorobutanesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-(3-phenylprop-2-enoyl)naphthalen-2-yl nonafluorobutanesulfonate(960505-59-3)
EPA Substance Registry System: (E)-1-(3-phenylprop-2-enoyl)naphthalen-2-yl nonafluorobutanesulfonate(960505-59-3)

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: 960505-59-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 960505-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,5,0 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 960505-59:
(8*9)+(7*6)+(6*0)+(5*5)+(4*0)+(3*5)+(2*5)+(1*9)=173
173 % 10 = 3
So 960505-59-3 is a valid CAS Registry Number.

960505-59-3Upstream product

960505-59-3Downstream Products

960505-59-3Relevant academic research and scientific papers

Synthesis of chiral 3-substituted indanones via an enantioselective reductive-heck reaction

Minatti, Ana,Zheng, Xiaolai,Buchwald, Stephen L.

, p. 9253 - 9258 (2008/03/13)

(Chemical Equation Presented) An efficient intramolecular palladium-catalyzed, asymmetric reductive-Heck reaction has been developed, which allowed for the synthesis of either enantiomerically enriched 3-substituted indanones or α-exo-methylene indanones depending on the base used.

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