Cas 122271-72-1,Trifluoro-methanesulfonate2-diethylamino-4-phenyl-1,3-bis-trimethylsilanyl-2,3-dihydro-[1,3,2]diazaphosphet-1-ium;

122271-72-1

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Basic information

Product Name: Trifluoro-methanesulfonate2-diethylamino-4-phenyl-1,3-bis-trimethylsilanyl-2,3-dihydro-[1,3,2]diazaphosphet-1-ium;
Synonyms:
CAS NO:122271-72-1
Molecular Formula:
Molecular Weight: 515.684
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: Trifluoro-methanesulfonate2-diethylamino-4-phenyl-1,3-bis-trimethylsilanyl-2,3-dihydro-[1,3,2]diazaphosphet-1-ium;(CAS DataBase Reference)
NIST Chemistry Reference: Trifluoro-methanesulfonate2-diethylamino-4-phenyl-1,3-bis-trimethylsilanyl-2,3-dihydro-[1,3,2]diazaphosphet-1-ium;(122271-72-1)
EPA Substance Registry System: Trifluoro-methanesulfonate2-diethylamino-4-phenyl-1,3-bis-trimethylsilanyl-2,3-dihydro-[1,3,2]diazaphosphet-1-ium;(122271-72-1)

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: 122271-72-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 122271-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,7 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122271-72:
(8*1)+(7*2)+(6*2)+(5*2)+(4*7)+(3*1)+(2*7)+(1*2)=91
91 % 10 = 1
So 122271-72-1 is a valid CAS Registry Number.

122271-72-1Upstream product

24261-90-3 N,N,N'-tris(trimethylsilyl)benzamidine

122271-72-1Downstream Products

122271-72-1Relevant academic research and scientific papers

Phosphenium Cations in Heterocyclic Chemistry

Mazieres, M. R.,Roques, C.,Khim, T.,Majoral, J. P.,Wolf, R.,Sanchez, M.

, p. 309 - 312 (2007/10/02)

In the singlet state phosphenium cations feature both a vacant orbital and a lone pair at the phosphorus center (1).The anticipated amphoterism property of these species can be used for the synthesis of unusual heterocyclic derivatives.Our interest (2) in

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