Bis(diethylamino)chlorophosphine
Names
[ CAS No. ]:
685-83-6
[ Name ]:
Bis(diethylamino)chlorophosphine
[Synonym ]:
MFCD00015493
Bisdiethylamino-chloro-phosphine
tetraethyldiamidophosphorous acid chloride
Phosphorodiamidous chloride, tetraethyl-
N,N,N',N'-Tetraethylphosphorodiamidous chloride
tetraethyldiamidophophorous acid chloride
Bdapcd
Phosphorodiamidous chloride, N,N,N',N'-tetraethyl-
Bis(diethylamino)chlorophosphine
Chemical & Physical Properties
[ Density]:
1.002 g/mL at 25 °C(lit.)
[ Boiling Point ]:
235.3±23.0 °C at 760 mmHg
[ Molecular Formula ]:
C8H20ClN2P
[ Molecular Weight ]:
210.685
[ Flash Point ]:
96.1±22.6 °C
[ Exact Mass ]:
210.105255
[ PSA ]:
20.07000
[ LogP ]:
3.52
[ Vapour Pressure ]:
0.1±0.5 mmHg at 25°C
[ Index of Refraction ]:
n20/D 1.4895(lit.)
MSDS
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H314
[ Supplemental HS ]:
Reacts violently with water.
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
C:Corrosive;
[ Risk Phrases ]:
R14;R34
[ Safety Phrases ]:
S23-S26-S36-S36/37/39-S45
[ RIDADR ]:
UN 3265 8/PG 2
[ WGK Germany ]:
3
[ Packaging Group ]:
II
[ Hazard Class ]:
8
[ HS Code ]:
2929909090
Synthetic Route
Customs
[ HS Code ]: 2929909090
[ Summary ]:
2929909090 other compounds with other nitrogen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
Articles
Bioconjug. Chem. 1(5) , 319-24, (1990)
The synthesis of a self-complementary oligonucleotide possessing an anthraquinonylmethyl substituent at the designated sugar fragment, 5'-CCU(2'AQ)AGCTAGG (1), is described. The anthraquinonylmethyl g...
A phosphorbisamidite approach to the synthesis of oligodeoxyribonucleotides and their analogues.Nucleic Acids Symp. Ser. (21) , 31-2, (1989)
Utilities of deoxyribonucleoside 3'-O-phosphorbisdiethylamidites in the synthesis of oligodeoxyribonucleotides and their analogues are described.