Cas 220960-95-2,(10R,11R)-10,11-dimethoxy-10,11-dihydrodibenzo[b,f]thiepine

220960-95-2

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Basic information

Product Name: (10R,11R)-10,11-dimethoxy-10,11-dihydrodibenzo[b,f]thiepine
Synonyms: (10R,11R)-10,11-dimethoxy-10,11-dihydrodibenzo[b,f]thiepine
CAS NO:220960-95-2
Molecular Formula:
Molecular Weight: 272.368
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: (10R,11R)-10,11-dimethoxy-10,11-dihydrodibenzo[b,f]thiepine(CAS DataBase Reference)
NIST Chemistry Reference: (10R,11R)-10,11-dimethoxy-10,11-dihydrodibenzo[b,f]thiepine(220960-95-2)
EPA Substance Registry System: (10R,11R)-10,11-dimethoxy-10,11-dihydrodibenzo[b,f]thiepine(220960-95-2)

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: 220960-95-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220960-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,9,6 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 220960-95:
(8*2)+(7*2)+(6*0)+(5*9)+(4*6)+(3*0)+(2*9)+(1*5)=122
122 % 10 = 2
So 220960-95-2 is a valid CAS Registry Number.

220960-95-2Upstream product

181658-27-5 (1R,2R)-1,2-bis(2'-bromophenyl)-1,2-dimethoxyethane

220960-95-2Downstream Products

220960-95-2Relevant academic research and scientific papers

Synthesis and chemistry of enantiomerically pure 10,11-dihydrodibenzo[b,f] thiepines

Wyatt, Paul,Hudson, Andrew,Charmant, Jonathan,Orpen, A. Guy,Phetmung, Hirihattaya

, p. 2218 - 2232 (2006)

Several chiral thiepines were efficiently constructed using sulfur diimidazole in combination with a variety of bislithiated carbon fragments. The sulfur atom in these thiepines is found to be unusually unreactive compared to diphenylsulfide. The Royal Society of Chemistry 2006.

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