2,2,2-Trichloroethoxysulfonamide
Modify Date: 2024-01-08 11:00:49
2,2,2-Trichloroethoxysulfonamide structure
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Common Name | 2,2,2-Trichloroethoxysulfonamide | ||
|---|---|---|---|---|
| CAS Number | 69226-51-3 | Molecular Weight | 228.48200 | |
| Density | 1.801g/cm3 | Boiling Point | 288.7ºC at 760 mmHg | |
| Molecular Formula | C2H4Cl3NO3S | Melting Point | 56 °C | |
| MSDS | Chinese USA | Flash Point | 128.4ºC | |
| Name | 2,2,2-trichloroethyl sulfamate |
|---|---|
| Synonym | More Synonyms |
| Density | 1.801g/cm3 |
|---|---|
| Boiling Point | 288.7ºC at 760 mmHg |
| Melting Point | 56 °C |
| Molecular Formula | C2H4Cl3NO3S |
| Molecular Weight | 228.48200 |
| Flash Point | 128.4ºC |
| Exact Mass | 226.89800 |
| PSA | 77.77000 |
| LogP | 2.35780 |
| Index of Refraction | 1.543 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| RIDADR | NONH for all modes of transport |
| RTECS | WO6200000 |
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~88%
2,2,2-Trichloro... CAS#:69226-51-3 |
| Literature: Fiori, Kristin Williams; Du Bois Journal of the American Chemical Society, 2007 , vol. 129, # 3 p. 562 - 568 |
|
~52%
2,2,2-Trichloro... CAS#:69226-51-3 |
| Literature: Yamamoto, Hirofumi; Ho, Elisabeth; Sasaki, Ikuo; Mitsutake, Mizuho; Takagi, Yuichi; Imagawa, Hiroshi; Nishizawa, Mugio European Journal of Organic Chemistry, 2011 , # 13 p. 2417 - 2420 |
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~%
2,2,2-Trichloro... CAS#:69226-51-3 |
| Literature: Sbihi; Beji; Baklouti Journal of Fluorine Chemistry, 2002 , vol. 115, # 2 p. 161 - 164 |
|
~%
2,2,2-Trichloro... CAS#:69226-51-3 |
| Literature: Bess, Elizabeth N.; Deluca, Ryan J.; Tindall, Daniel J.; Oderinde, Martins S.; Roizen, Jennifer L.; Du Bois; Sigman, Matthew S. Journal of the American Chemical Society, 2014 , vol. 136, # 15 p. 5783 - 5789 |
CAS#:5329-14-6|
Catalytic intermolecular amination of C-H bonds: method development and mechanistic insights.
J. Am. Chem. Soc. 129 , 562, (2007) Reaction methodology for intermolecular C-H amination of benzylic and 3 degrees C-H bonds is described. This process uses the starting alkane as the limiting reagent, gives optically pure tetrasubstit... |
| sulfamate de trichloro-2,2,2 ethyle |
| CCl3CH2OSO2NH2 |
| 2,2,2-trichloroethoxysulfonyl amine |
| 1,1,1-trichloroethylsulfamate ester |
| 2,2,2-Trichloroethoxysulfonamide |
| Sulfamic acid,2,2,2-trichloroethyl ester |
| 2,2,2,3',4'-PENTAFLUOROACETOPHENONE |