Cas 756-66-1,germanamine, N,N,1,1,1-pentaethyl-

756-66-1

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Basic information

Product Name: germanamine, N,N,1,1,1-pentaethyl-
Synonyms: N,N,1,1,1-Pentaethylgermanamine
CAS NO:756-66-1
Molecular Formula: C₁₀H₂₅GeN
Molecular Weight: 231.9522
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 220.014°C at 760 mmHg
Flash Point: 76.334°C
Appearance: N/A
Density: N/A
Vapor Pressure: 0.116mmHg at 25°C
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: germanamine, N,N,1,1,1-pentaethyl-(CAS DataBase Reference)
NIST Chemistry Reference: germanamine, N,N,1,1,1-pentaethyl-(756-66-1)
EPA Substance Registry System: germanamine, N,N,1,1,1-pentaethyl-(756-66-1)

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: 756-66-1(Hazardous Substances Data)

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756-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 756-66-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 756-66:
(5*7)+(4*5)+(3*6)+(2*6)+(1*6)=91
91 % 10 = 1
So 756-66-1 is a valid CAS Registry Number.

756-66-1Upstream product

209072-05-9 (C₂H₅)3Ge(SO₃CF₃)

756-66-1Downstream Products

756-66-1Relevant academic research and scientific papers

Synthese de germyl perfluoroalcanes sulfonates. Quelques aspects de leur reactivite en tant qu'agent de germylation

Castany,Lavayssiere,Dousse

, p. 781 - 801 (2008/10/09)

Trifluoromethanesulfonates of germanium(IV) and (II) have been synthesized by reacting triflic acid or silver triflate with several functional organogermanes. Their characterization by 1H, 13C, 19F NMR, IR and mass spectrometry is described. The reactivity with neutral or charged nucleophiles (protic and aprotic) has also been studied. In the case of neutral nucleophiles, the reaction appeared to be a good method for germylation of enolizable ketones and esters.

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