Name: TETRAETHYLAMMONIUM CYANIDE
SKU: 13435-20-6

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Basic Information

CAS No.:

13435-20-6

Name:

TETRAETHYLAMMONIUM CYANIDE

Article Data:

Molecular Structure:

Formula:

C8 H20 N

Molecular Weight:

156.271

Synonyms:

Ammonium,tetraethyl-, cyanide (8CI); Ethanaminium, N,N,N-triethyl-, cyanide (9CI);Tetraethylammonium cyanide (7CI)

Density:

g/cm³

Melting Point:

250 °C (dec.)(lit.)

Boiling Point:

°Cat760mmHg

Flash Point:

°C

Hazard Symbols:

Risk Codes:

26/27/28-32-50/53

Safety:

Hazard Codes	T+,N
Risk Statements	26/27/28-32-50/53
Safety Statements	7-28-29-45-60-61
RIDADR	UN 2811 6.1/PG 2
WGK Germany	3
F	3-8-10
HazardClass	6.1(b)
PackingGroup	III

PSA:

23.79000

LogP:

1.97918

Synthetic route

: potassium cyanide

: 56-34-8
tetraethylammonium chloride

: 13435-20-6
tetraethylammoniumcyanide

Conditions

Conditions	Yield
In water for 1h; Reflux;	79%

: 56-34-8
tetraethylammonium chloride

NaCN: NaCN

: 13435-20-6
tetraethylammoniumcyanide

Conditions

Conditions	Yield
In methanol	50.6%

: 19099-54-8
2-isopropyliodobenzene

: 13435-20-6
tetraethylammoniumcyanide

: 544-92-3
copper(I) cyanide

: 40751-52-8
2-Isopropyl-1-benzonitrile

Conditions

Conditions	Yield
1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0) In tetrahydrofuran for 1.5h; Heating / reflux;	100%

...Expand

: 929016-41-1
C15H23ClN4O4

: 13435-20-6
tetraethylammoniumcyanide

: 929015-78-1
methyl 2-cyano-6-[2-{[(1,1-dimethylethyl)oxy]carbonyl}-1-(2-methylpropyl)hydrazino]-4-pyrimidinecarboxylate

Conditions

Conditions	Yield
With trimethylamine In tetrahydrofuran at -78 - 20℃; for 24h;	100%

: 12702-09-9
thorium di-π-cyclooctatetraene

: 13435-20-6
tetraethylammoniumcyanide

: CN(1-)*C8H20N(1+)*Th(4+)*2C8H8(2-)

Conditions

Conditions	Yield
With pyridine for 15h; Reflux; Inert atmosphere;	100%

: syn-[Mo2O2(μ-S)2(S2)(DMF)3]

: 13435-20-6
tetraethylammoniumcyanide

: C3Mo2N3O2S4(3-)*3C8H20N(1+)

Conditions

Conditions	Yield
In acetonitrile at 0℃;	100%

: dicarbonyl(cyclopentadienyl)(ethyl vinyl ether)iron tetrafluoroborate

: 13435-20-6
tetraethylammoniumcyanide

: 2-cyano-2-ethoxyethyldicarbonyl-η-cyclopentadienyliron(II)

Conditions

Conditions	Yield
In dichloromethane byproducts: tetraethylammonium tetrafluoroborate; Et4NCN (5% xs) was added to a soln. of Fe-complex in CH2Cl2 under Ar at 0°C, mixt. was stirred for 0.5 h; ether was added, soln. was filtered through a short plug of alumina to remove Et4NBF4, evapd. in vacuo; elem. anal.;	99%

: 1,3-(μ-propanedithiolato)diironhexacarbonyl

: 13435-20-6
tetraethylammoniumcyanide

: 2N(C2H5)4(1+)*[Fe(CO)2CN]2SC3H6S(2-)*H2O=[N(C2H5)4]2[Fe(CO)2CN]2SC3H6S*H2O

Conditions

Conditions	Yield
In acetonitrile room temp.; elem. anal.;	99%

: Mo2O5(O2C6H2(NCHC6H3(OC2H5)O)2Ni)2

: 13435-20-6
tetraethylammoniumcyanide

: 2N(C2H5)4(1+)*2MoO2(2+)*O(2-)*2Ni(2+)*2CN(1-)*2O2C6H2(NCHC6H3(OC2H5)O)2(3-)=[N(C2H5)4]2[((CN)Ni(C24H20N2O6)MoO2)2O]

Conditions

Conditions	Yield
In nitromethane; dichloromethane inert atmosphere; 2 equiv. Et4NCN, stirring in CH2Cl2/MeNO2=1:1 for 1 h (dissoln.); filtration, crystn. on layering with Et2O (overnight), collection (filtration; elem. anal.;	99%