Cas 129303-11-3,(4aR,7aS)-7a-Hydroxy-3,4a-dimethyl-3-phenylsulfanylmethyl-hexahydro-cyclopenta[c][1,2]dioxin-5-one

129303-11-3

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Basic information

Product Name: (4aR,7aS)-7a-Hydroxy-3,4a-dimethyl-3-phenylsulfanylmethyl-hexahydro-cyclopenta[c][1,2]dioxin-5-one
Synonyms: (4aR,7aS)-7a-Hydroxy-3,4a-dimethyl-3-phenylsulfanylmethyl-hexahydro-cyclopenta[c][1,2]dioxin-5-one
CAS NO:129303-11-3
Molecular Formula:
Molecular Weight: 308.398
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: (4aR,7aS)-7a-Hydroxy-3,4a-dimethyl-3-phenylsulfanylmethyl-hexahydro-cyclopenta[c][1,2]dioxin-5-one(CAS DataBase Reference)
NIST Chemistry Reference: (4aR,7aS)-7a-Hydroxy-3,4a-dimethyl-3-phenylsulfanylmethyl-hexahydro-cyclopenta[c][1,2]dioxin-5-one(129303-11-3)
EPA Substance Registry System: (4aR,7aS)-7a-Hydroxy-3,4a-dimethyl-3-phenylsulfanylmethyl-hexahydro-cyclopenta[c][1,2]dioxin-5-one(129303-11-3)

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: 129303-11-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129303-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,3,0 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 129303-11:
(8*1)+(7*2)+(6*9)+(5*3)+(4*0)+(3*3)+(2*1)+(1*1)=103
103 % 10 = 3
So 129303-11-3 is a valid CAS Registry Number.

129303-11-3Upstream product

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129303-11-3Relevant academic research and scientific papers

Oxygenation of γ,δ-unsaturated ketones in the presence of thiophenol. Efficient formation of cyclic peroxides

Yoshida, Jun-Ichi,Nakatani, Shogo,Isoe, Sachihiko

, p. 2425 - 2428 (1990)

γ,δ-Unsaturated ketones were found to be oxygenated in the presence of thiophenol to give the corresponding cyclic peroxides. The electrochemical initiation accelerated the reaction markedly.

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