Cas 501700-70-5,(1S,4R,6R,8R)-11,11-dimethyl-4-[(E)-2-phenyl-propenyl]-5-oxa-3-thia-tricyclo[6.2.1.0<sup>1,6</sup>]undecane

501700-70-5

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Basic information

Product Name: (1S,4R,6R,8R)-11,11-dimethyl-4-[(E)-2-phenyl-propenyl]-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane
Synonyms: (1S,4R,6R,8R)-11,11-dimethyl-4-[(E)-2-phenyl-propenyl]-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane
CAS NO:501700-70-5
Molecular Formula:
Molecular Weight: 314.492
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: (1S,4R,6R,8R)-11,11-dimethyl-4-[(E)-2-phenyl-propenyl]-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane(CAS DataBase Reference)
NIST Chemistry Reference: (1S,4R,6R,8R)-11,11-dimethyl-4-[(E)-2-phenyl-propenyl]-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane(501700-70-5)
EPA Substance Registry System: (1S,4R,6R,8R)-11,11-dimethyl-4-[(E)-2-phenyl-propenyl]-5-oxa-3-thia-tricyclo[6.2.1.0^1,6]undecane(501700-70-5)

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: 501700-70-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 501700-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,7,0 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 501700-70:
(8*5)+(7*0)+(6*1)+(5*7)+(4*0)+(3*0)+(2*7)+(1*0)=95
95 % 10 = 5
So 501700-70-5 is a valid CAS Registry Number.

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501700-70-5Relevant academic research and scientific papers

Ketene Claisen rearrangement of camphor-derived 1,3-oxathianes: Complete control of tertiary and quaternary stereogenic centres

Aggarwal, Varinder K.,Lattanzi, Alessandra,Fuentes, Daniel

, p. 2534 - 2535 (2002)

Dichloroketene reacts, via a [3,3]-sigmatropic rearrangement, with camphor-derived 1,3-oxathianes of α,β-unsaturated aldehydes to give macrocyclic thiolactones in high yield and with complete transfer of chirality. The rearrangement is stereospecific.

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