| Company Name: |
BOC Sciences |
| Tel: |
1-631-485-4226; 16314854226 |
| Email: |
info@bocsci.com |
| Company Name: |
BOC Sciences |
| Tel: |
16314854226 |
| Email: |
info@bocsci.com |
|
| | N-Methyl Etodolac Basic information |
| Product Name: | N-Methyl Etodolac | | Synonyms: | 1,8-Diethyl-1,3,4,9-tetrahydro-9-methyl-pyrano[3,4]indole-1-acetic Aci;N-Methyl Etodolac;1,8-Diethyl-1,3,4,9-tetrahydro-9-methyl-pyrano[3,4]indole-1-acetic Acid;Etodolac Impurity 25 (N-Methyl Etodolac);Etodolac Impurity 13;Etodolac Impurity 12;Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-9-methyl-;Etoronic acid impurity 13 | | CAS: | 849630-94-0 | | MF: | C18H23NO3 | | MW: | 301.38 | | EINECS: | | | Product Categories: | Heterocycles;Amines;Indole Derivatives;Intermediates & Fine Chemicals;Pharmaceuticals | | Mol File: | 849630-94-0.mol |  |
| | N-Methyl Etodolac Chemical Properties |
| Boiling point | 507.9±45.0 °C(Predicted) | | density | 1.19±0.1 g/cm3(Predicted) | | pka | 4.31±0.10(Predicted) |
| | N-Methyl Etodolac Usage And Synthesis |
| Uses | An indole derivative for treatment of multiple myeloma | | Uses | N-Methyl Etodolac is used in the preparation of indole derivatives as COX-1-, COX-2-, and β-catenin-inhibitors for treatment of multiple myeloma. |
| | N-Methyl Etodolac Preparation Products And Raw materials |
|