| Company Name: |
Energy Chemical |
| Tel: |
400-0056266 |
| Email: |
marketing1@energy-chemical.com |
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| | 3'-hydroxy-4'-methoxydiclofenac Basic information |
| Product Name: | 3'-hydroxy-4'-methoxydiclofenac | | Synonyms: | 3'-hydroxy-4'-methoxydiclofenac;[2-(2,6-Dichloro-3-hydroxy-4-methoxyanilino)phenyl]acetic acid;2-(2,6-Dichloro-3-hydroxy-4-methoxyphenylamino)benzeneacetic acid;YALZBLAHGKGDMB-UHFFFAOYSA-N;Diclofenac sodium Impurity 49;Diclofenac Impurity 29;Diazoxide Impurity 7;3′-Hydroxy-4′-methoxydiclofenac, CAS 106610-60-0 | | CAS: | 106610-60-0 | | MF: | C15H13Cl2NO4 | | MW: | 0 | | EINECS: | | | Product Categories: | | | Mol File: | 106610-60-0.mol |  |
| | 3'-hydroxy-4'-methoxydiclofenac Chemical Properties |
| Melting point | >166°C (dec.) | | storage temp. | Refrigerator | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Solid | | color | White to Off-White |
| | 3'-hydroxy-4'-methoxydiclofenac Usage And Synthesis |
| Uses | 3''-Hydroxy-4''-methoxydiclofenac is a derivative of Diclofenac (Sodium Salt: D436450). Diclofenac is the first non-steroidal anti-inflammatory drug (NSAID) that is derived from phenylacetic acid. Diclofenac, like other NSAIDs, primarily works by targeting the cyclo-oxygenase pathway in the arachidonic acid cascade, reducing the formation of inflammation mediators in the body. | | Definition | ChEBI: An organochlorine compound that is a metabolite of diclofenac having hydroxy and methoxy groups at positions 3' and 4' respectively.. |
| | 3'-hydroxy-4'-methoxydiclofenac Preparation Products And Raw materials |
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