2,2,2-Trichloroacetamide structure
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Common Name | 2,2,2-Trichloroacetamide | ||
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CAS Number | 594-65-0 | Molecular Weight | 162.402 | |
Density | 1.7±0.1 g/cm3 | Boiling Point | 239.0±0.0 °C at 760 mmHg | |
Molecular Formula | C2H2Cl3NO | Melting Point | 139-141 °C(lit.) | |
MSDS | USA | Flash Point | 88.5±25.9 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 2,2,2-Trichloroacetamide |
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Synonym | More Synonyms |
Density | 1.7±0.1 g/cm3 |
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Boiling Point | 239.0±0.0 °C at 760 mmHg |
Melting Point | 139-141 °C(lit.) |
Molecular Formula | C2H2Cl3NO |
Molecular Weight | 162.402 |
Flash Point | 88.5±25.9 °C |
Exact Mass | 160.920197 |
PSA | 43.09000 |
LogP | 1.15 |
Vapour Pressure | 0.0±0.4 mmHg at 25°C |
Index of Refraction | 1.521 |
Stability | Stable. Incompatible with strong acids, strong bases, strong oxidizing agents, strong reducing agents. |
Water Solubility | 13 g/L (20 ºC) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H319 |
Precautionary Statements | P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn:Harmful; |
Risk Phrases | R22;R36/37/38 |
Safety Phrases | S36/37-S45-S37/39-S26 |
RIDADR | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
RTECS | AC9275000 |
Hazard Class | 6.1 |
HS Code | 29241900 |
Precursor 8 | |
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DownStream 10 | |
HS Code | 2924199090 |
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Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
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J. Org. Chem. 78(4) , 1699-705, (2013) We describe an improved synthesis of (-)-5,11-dideoxytetrodotoxin from an enone, which was used for synthesis of tetrodotoxin and its analogues in this laboratory. One of the major modifications was t... |
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Activation of glycosyl trichloroacetimidates with perchloric acid on silica (HClO(4)-SiO(2)) provides enhanced alpha-selectivity.
Carbohydr. Res. 345(14) , 2074-8, (2010) Obtaining high stereoselectivity in glycosylation reactions is often challenging in the absence of neighboring group participation. In this study, we demonstrate that activation of glycosyl trichloroa... |
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Acetamide, 2,2,2-trichloro- |
TRICHLOROACETAMIDE |
2,2,2-Trichloroacetamide |
3,3,3-trichloroacetamide |
chloraloxime |
2,2,13,13-TETRAMETHYL-4,7,11-TRIOXO-3,12-DIOXA-5,8-DIAZATETRADECANE-6-CARBOXYLIC ACID |
2,2,2-Chloroacetamide |
a,a,a-Trichloroacetamide |
trichloro-acetic acid amide |
2,2,2-Trichloroaceta |
trichloroacetyl amide |
MFCD00008009 |
EINECS 209-849-3 |
2,2,2-trichloro-acetamid |
Trichloroacetaldoxime |
2,2,2-trichloro-acetamide |
Trichloroacetimidic acid |