Cas 97985-05-2,(3S,4R)-3-{(E)-(S)-1-[(E)-2-((S)-Benzenesulfinyl)-vinyl]-but-2-enyl}-4-tert-butoxy-cyclopentanone

97985-05-2

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Basic information

Product Name: (3S,4R)-3-{(E)-(S)-1-[(E)-2-((S)-Benzenesulfinyl)-vinyl]-but-2-enyl}-4-tert-butoxy-cyclopentanone
Synonyms: (3S,4R)-3-{(E)-(S)-1-[(E)-2-((S)-Benzenesulfinyl)-vinyl]-but-2-enyl}-4-tert-butoxy-cyclopentanone
CAS NO:97985-05-2
Molecular Formula:
Molecular Weight: 360.518
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: (3S,4R)-3-{(E)-(S)-1-[(E)-2-((S)-Benzenesulfinyl)-vinyl]-but-2-enyl}-4-tert-butoxy-cyclopentanone(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-3-{(E)-(S)-1-[(E)-2-((S)-Benzenesulfinyl)-vinyl]-but-2-enyl}-4-tert-butoxy-cyclopentanone(97985-05-2)
EPA Substance Registry System: (3S,4R)-3-{(E)-(S)-1-[(E)-2-((S)-Benzenesulfinyl)-vinyl]-but-2-enyl}-4-tert-butoxy-cyclopentanone(97985-05-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 97985-05-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97985-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,8 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97985-05:
(7*9)+(6*7)+(5*9)+(4*8)+(3*5)+(2*0)+(1*5)=202
202 % 10 = 2
So 97985-05-2 is a valid CAS Registry Number.

97985-05-2Upstream product

97985-05-2Downstream Products

97985-05-2Relevant academic research and scientific papers

THE DIASTEREOSPECIFIC APROTIC CONJUGATE ADDITION REACTIONS OF CARBANIONS DERIVED FROM ALLYLIC SULFOXIDES AND ALLYLIC PHOSPHINE OXIDES.

Binns, Malcolm R.,Haynes, Richard K.,Katsifis, Andrew A.,Schober, Paul A.,Vonwiller, Simone C.

, p. 1565 - 1568 (1985)

The title carbanions undergo conjugate addition to cyclic enones in THF to deliver vinylic sulfoxides and vinylic phosphine oxides as single diastereomers.

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