| Weight | 197.832 g/mol |
|---|---|
| Formula | C2Cl4O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
DIPHOSGENE (503-38-8)
trichloromethyl chloroformate
Score:
#1186 in Physics
,
#3372 in Chemistry
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- Isocyanide Synthesis with Diphosgene (Angewandte Chemie, 1977)
- An improved rapid method for the synthesis of N-carboxy .alpha.-amino acid anhydrides using trichloromethyl chloroformate (Journal of Organic Chemistry, 1985)
- Poly(anhydrides). 2. One-step polymerization using phosgene or diphosgene as coupling agents (Macromolecules, 1988)
- Conversion of Bis(trichloromethyl) Carbonate to Phosgene and Reactivity of Triphosgene, Diphosgene, and Phosgene with Methanol1 (Journal of Organic Chemistry, 2000)
- Trichloromethyl chloroformate. Reaction with amines, amino acids, and amino alcohols (Journal of Organic Chemistry, 1976)
- Synthesis of some aromatic diisocyanides with trichloromethyl chloroformate (Journal of Organic Chemistry, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - trichloromethyl chloroformate
-
SMILESC(=O)(OC(Cl)(Cl)Cl)Cl
-
InChIKeyHCUYBXPSSCRKRF-UHFFFAOYSA-N
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