Cas 98796-80-6,(1S,3R,4R,6R)-3-Chloro-3,7,7-trimethyl-4-phenylsulfanyl-bicyclo[4.1.0]heptane

98796-80-6

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Basic information

Product Name: (1S,3R,4R,6R)-3-Chloro-3,7,7-trimethyl-4-phenylsulfanyl-bicyclo[4.1.0]heptane
Synonyms: (1S,3R,4R,6R)-3-Chloro-3,7,7-trimethyl-4-phenylsulfanyl-bicyclo[4.1.0]heptane
CAS NO:98796-80-6
Molecular Formula:
Molecular Weight: 280.862
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,3R,4R,6R)-3-Chloro-3,7,7-trimethyl-4-phenylsulfanyl-bicyclo[4.1.0]heptane(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3R,4R,6R)-3-Chloro-3,7,7-trimethyl-4-phenylsulfanyl-bicyclo[4.1.0]heptane(98796-80-6)
EPA Substance Registry System: (1S,3R,4R,6R)-3-Chloro-3,7,7-trimethyl-4-phenylsulfanyl-bicyclo[4.1.0]heptane(98796-80-6)

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: 98796-80-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98796-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,9 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98796-80:
(7*9)+(6*8)+(5*7)+(4*9)+(3*6)+(2*8)+(1*0)=216
216 % 10 = 6
So 98796-80-6 is a valid CAS Registry Number.

98796-80-6Upstream product

98796-80-6Downstream Products

98796-80-6Relevant academic research and scientific papers

NUCLEOPHILIC SUBSTITUTION IN β-CHLORO(ALKYLTHIO)CARANES, OBTAINED BY ELECTROPHILIC CHLOROSULFENYLATION OF 3-CARENE

Plemenkov, V. V.,Bairamova, F. A.,Butenko, G. G.,Artemova, N. P.,Litvinov, I. A.,et al.

, p. 869 - 874 (2007/10/02)

3-Chloro-4-methylthiocarane, obtained by electrophilic chlorosulfenylation of 3-carene, was brought into nucleophilic substitution, and the functional derivatives of the methylthiocaranes were converted into the corresponding sulfones.Substitution of the

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