Cas 1058672-07-3,(R)-1,1,1,3,3,3-hexafluoropropan-2-yl 1-(3-(naphthalen-1-ylthio)-3-oxopropyl)-2-oxocyclohexanecarboxylate

1058672-07-3

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Basic information

Product Name: (R)-1,1,1,3,3,3-hexafluoropropan-2-yl 1-(3-(naphthalen-1-ylthio)-3-oxopropyl)-2-oxocyclohexanecarboxylate
Synonyms: (R)-1,1,1,3,3,3-hexafluoropropan-2-yl 1-(3-(naphthalen-1-ylthio)-3-oxopropyl)-2-oxocyclohexanecarboxylate
CAS NO:1058672-07-3
Molecular Formula:
Molecular Weight: 506.466
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: (R)-1,1,1,3,3,3-hexafluoropropan-2-yl 1-(3-(naphthalen-1-ylthio)-3-oxopropyl)-2-oxocyclohexanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1,1,1,3,3,3-hexafluoropropan-2-yl 1-(3-(naphthalen-1-ylthio)-3-oxopropyl)-2-oxocyclohexanecarboxylate(1058672-07-3)
EPA Substance Registry System: (R)-1,1,1,3,3,3-hexafluoropropan-2-yl 1-(3-(naphthalen-1-ylthio)-3-oxopropyl)-2-oxocyclohexanecarboxylate(1058672-07-3)

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: 1058672-07-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1058672-07-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,6,7 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1058672-07:
(9*1)+(8*0)+(7*5)+(6*8)+(5*6)+(4*7)+(3*2)+(2*0)+(1*7)=163
163 % 10 = 3
So 1058672-07-3 is a valid CAS Registry Number.

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1058672-07-3Relevant academic research and scientific papers

Enantioselective organocatalytic Michael additions to acrylic acid derivatives: Generation of all-carbon quaternary stereocentres

Rigby, Caroline L.,Dixon, Darren J.

, p. 3798 - 3800 (2008)

Acrylic esters, thioesters and N-acryloyl pyrrole have been identified as effective electrophiles in the enantioselective Michael addition reaction with β-keto ester pro-nucleophiles catalysed by a cinchona alkaloid derived bifunctional organocatalyst; enantiomeric excesses of up to 98% and yields of up to 96% can be obtained for a range of Michael acceptors and pro-nucleophiles. The Royal Society of Chemistry.

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