Cas 132713-29-2,(S)-2,2-Dimethyl-4-[(1R,2R,3R)-2-methyl-2-(2-phenylsulfanyl-ethyl)-3-((R)-1-phenylsulfanylmethyl-pent-4-enyl)-cyclopentyl]-[1,3]dioxolane

132713-29-2

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Basic information

Product Name: (S)-2,2-Dimethyl-4-[(1R,2R,3R)-2-methyl-2-(2-phenylsulfanyl-ethyl)-3-((R)-1-phenylsulfanylmethyl-pent-4-enyl)-cyclopentyl]-[1,3]dioxolane
Synonyms: (S)-2,2-Dimethyl-4-[(1R,2R,3R)-2-methyl-2-(2-phenylsulfanyl-ethyl)-3-((R)-1-phenylsulfanylmethyl-pent-4-enyl)-cyclopentyl]-[1,3]dioxolane
CAS NO:132713-29-2
Molecular Formula:
Molecular Weight: 510.805
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: (S)-2,2-Dimethyl-4-[(1R,2R,3R)-2-methyl-2-(2-phenylsulfanyl-ethyl)-3-((R)-1-phenylsulfanylmethyl-pent-4-enyl)-cyclopentyl]-[1,3]dioxolane(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2,2-Dimethyl-4-[(1R,2R,3R)-2-methyl-2-(2-phenylsulfanyl-ethyl)-3-((R)-1-phenylsulfanylmethyl-pent-4-enyl)-cyclopentyl]-[1,3]dioxolane(132713-29-2)
EPA Substance Registry System: (S)-2,2-Dimethyl-4-[(1R,2R,3R)-2-methyl-2-(2-phenylsulfanyl-ethyl)-3-((R)-1-phenylsulfanylmethyl-pent-4-enyl)-cyclopentyl]-[1,3]dioxolane(132713-29-2)

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: 132713-29-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132713-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,1 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132713-29:
(8*1)+(7*3)+(6*2)+(5*7)+(4*1)+(3*3)+(2*2)+(1*9)=102
102 % 10 = 2
So 132713-29-2 is a valid CAS Registry Number.

132713-29-2Upstream product

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132713-29-2Relevant academic research and scientific papers

A novel O-quinodimethane strategy for an active metabolite of vitamin D3. A total synthesis of 25-hydroxy Windaus-Grundmann ketone

Nemoto,Ando,Fukumoto

, p. 6205 - 6208 (2007/10/02)

A highly diastereoselective total synthesis of 25-hydroxy Windaus-Grundmann ketone (2) was achieved via a novel regiocontrolled C-C bond formation by an intramolecular epoxide ring opening reaction of the bissulfonyl epoxide (19) as a key step, which was

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