| Company Name: |
Energy Chemical |
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400-0056266 |
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sales8178@energy-chemical.com |
Ethyl 4-(2-chloroacetamido)benzoate manufacturers
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| | Ethyl 4-(2-chloroacetamido)benzoate Basic information |
| | Ethyl 4-(2-chloroacetamido)benzoate Chemical Properties |
| Melting point | 110-114 °C(lit.) | | Boiling point | 421.1±30.0 °C(Predicted) | | density | 1.283±0.06 g/cm3(Predicted) | | storage temp. | Inert atmosphere,Room Temperature | | pka | 12.36±0.70(Predicted) | | Appearance | White to off-white Solid | | InChI | 1S/C11H12ClNO3/c1-2-16-11(15)8-3-5-9(6-4-8)13-10(14)7-12/h3-6H,2,7H2,1H3,(H,13,14) | | InChIKey | ZVRJEYAQESBSSH-UHFFFAOYSA-N | | SMILES | CCOC(=O)c1ccc(NC(=O)CCl)cc1 |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26 | | WGK Germany | 3 | | HazardClass | IRRITANT | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | Ethyl 4-(2-chloroacetamido)benzoate Usage And Synthesis |
| Uses | Ethyl 4-(2-chloroacetamido)benzoate can be synthesized starting from benzocaine. It undergoes heterocyclization in the presence of ammonium thiocyanate in refluxing ethanol to afford ethyl-4-(4-oxothiazolidin-2-ylideneamino)benzoate, via intramolecular cyclization and the Dimroth-like rearrangements. | | General Description | Ethyl 4-(2-chloroacetamido)benzoate can be synthesized starting from benzocaine. It undergoes heterocyclization in the presence of ammonium thiocyanate in refluxing ethanol to afford ethyl-4-(4-oxothiazolidin-2-ylideneamino)benzoate, via intramolecular cyclization and the Dimroth-like rearrangements. |
| | Ethyl 4-(2-chloroacetamido)benzoate Preparation Products And Raw materials |
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