Cas 100830-68-0,2,2,2,2-tetracarbonyl-3,3-diphenyl-1-λ6-thia-3-phospha-2-rhenacyclooctane-S,S-dioxide

100830-68-0

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Basic information

Product Name: 2,2,2,2-tetracarbonyl-3,3-diphenyl-1-λ6-thia-3-phospha-2-rhenacyclooctane-S,S-dioxide
Synonyms: 2,2,2,2-tetracarbonyl-3,3-diphenyl-1-λ6-thia-3-phospha-2-rhenacyclooctane-S,S-dioxide
CAS NO:100830-68-0
Molecular Formula:
Molecular Weight: 617.633
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: 2,2,2,2-tetracarbonyl-3,3-diphenyl-1-λ6-thia-3-phospha-2-rhenacyclooctane-S,S-dioxide(CAS DataBase Reference)
NIST Chemistry Reference: 2,2,2,2-tetracarbonyl-3,3-diphenyl-1-λ6-thia-3-phospha-2-rhenacyclooctane-S,S-dioxide(100830-68-0)
EPA Substance Registry System: 2,2,2,2-tetracarbonyl-3,3-diphenyl-1-λ6-thia-3-phospha-2-rhenacyclooctane-S,S-dioxide(100830-68-0)

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: 100830-68-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 100830-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,3 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100830-68:
(8*1)+(7*0)+(6*0)+(5*8)+(4*3)+(3*0)+(2*6)+(1*8)=80
80 % 10 = 0
So 100830-68-0 is a valid CAS Registry Number.

100830-68-0Upstream product

100811-17-4 2,2,2,2-tetracarbonyl-1,1-diphenyl-1-phospha-2-rhenacycloheptane

100830-68-0Downstream Products

100830-68-0Relevant academic research and scientific papers

DARSTELLUNG UND EIGENSCHAFTEN VON DER REAKTIONEN MIT METALLHALTIGEN HETEROCYCLEN. XLVI. SYNTHESE, STRUKTUR UND CHEMISCHES VERHALTEN SIEBENGLIEDRIGER MANGANA- UND RHENACYCLOALKENE

Lindner, Ekkehard,Zinsser, Fritz,Hiller, Wolfgang,Fawzi, Riad

, p. 317 - 330 (2007/10/02)

The substitution compounds Br(OC)4MPPh2(CH2)nCl (M= Mn, Re; n= 5,6) are obtained by the action of the (5-chloropentyl- and 6-chlorohexyl)diphenylphosphanes Cl(CH2)nPPh2, which are formed from the α,ω-dihalogenoalkenes Cl(CH2)n/

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