Trichloroacetyl isocyanate
Names
[ CAS No. ]:
3019-71-4
[ Name ]:
Trichloroacetyl isocyanate
[Synonym ]:
Acetyl isocyanate, trichloro-
2,2,2-trichloroethanecarbonyl isocyanate
Acetyl isocyanate,trichloro
2,2,2-trichloro-acetyl isocyanate
EINECS 221-165-7
Trichloroacetyl isocyanate
trichloromethylcarbonylisocyanate
OCNVXGGG
Isocyanic Acid Trichloroacetyl Ester
2,2,2-Trichloroacetyl isocyanate
Trichloroacetyl isocyanate,NMR grade
MFCD00002033
Acetyl isocyanate, 2,2,2-trichloro-
Chemical & Physical Properties
[ Density]:
1.7±0.1 g/cm3
[ Boiling Point ]:
186.0±35.0 °C at 760 mmHg
[ Molecular Formula ]:
C3Cl3NO2
[ Molecular Weight ]:
188.397
[ Flash Point ]:
65.6±0.0 °C
[ Exact Mass ]:
186.899460
[ PSA ]:
46.50000
[ LogP ]:
2.38
[ Vapour Pressure ]:
0.7±0.4 mmHg at 25°C
[ Index of Refraction ]:
1.539
[ Storage condition ]:
2-8°C
MSDS
Safety Information
[ Symbol ]:
GHS05, GHS06, GHS08
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H311-H314-H331-H334
[ Supplemental HS ]:
Reacts violently with water.
[ Precautionary Statements ]:
P261-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 ]:
T:Toxic;
[ Risk Phrases ]:
R14;R23/24/25;R34;R42
[ Safety Phrases ]:
S23-S26-S36/37/39-S45-S8
[ RIDADR ]:
UN 2206 6.1/PG 3
[ WGK Germany ]:
3
[ Packaging Group ]:
II
[ Hazard Class ]:
6.1
[ HS Code ]:
2929109000
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2929109000
[ Summary ]:
2929109000. other isocyanates. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
J. Mol. Model. 8(2) , 44-9, (2002)
The conformational stability and vibrational infrared and Raman spectra of trichloroacetyl isocyanate (CCl3CONCO) were investigated by ab initio MP2 and density functional B3LYP calculations using the...
Improved catalytic and stereoselective glycosylation with glycosyl N-trichloroacetylcarbamate: application to various 1-hydroxy sugars.Carbohydr. Res. 345(6) , 740-9, (2010)
Efficient catalytic and stereoselective glycosylation was achieved by activating a glycosyl N-trichloroacetylcarbamate with a catalytic amount of Lewis acid in the presence of a glycosyl acceptor and ...
D.R. TaylorCan. J. Chem. 54 , 189, (1976)