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Tel: 17734809689
Tel: 17734809689
Tel: 86-371-86259723
Tel: 17734809689
Tel: 17734809689
Mobile: 17734809689
Tel: +86-371- 86259723
Fax: +86-371- 86259723
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| 3,5-DIHYDROXY-4-ACETYLTOLUENE Basic information |
| Product Name: | 3,5-DIHYDROXY-4-ACETYLTOLUENE |
| Synonyms: | 3,5-DIHYDROXY-4-ACETYLTOLUENE;2,6-DIHYDROXY-4'-METHYLACETOPHENONE;ETHANONE, 1-(2,6-DIHYDROXY-4-METHYLPHENYL)-;4-acetyl-3,5-dihydroxytoluene;4-ACETYL-3,5-DIHYDROXYTOLUENE,98.5+%;1-(2,6-Dihydroxy-4-methylphenyl)ethanone;p-Orcacetophenone;1-(2,6-dihydroxy-4-Methylphenyl)ethan-1-one |
| CAS: | 1634-34-0 |
| MF: | C9H10O3 |
| MW: | 166.17 |
| EINECS: | |
| Product Categories: | Alcohols and Derivatives;Carbonyl Compounds;Aromatic Acetophenones & Derivatives (substituted);Aromatics;Intermediates |
| Mol File: | 1634-34-0.mol |
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| 3,5-DIHYDROXY-4-ACETYLTOLUENE Chemical Properties |
| CAS DataBase Reference | 1634-34-0(CAS DataBase Reference) |
| Safety Information |
| 3,5-DIHYDROXY-4-ACETYLTOLUENE Usage And Synthesis |
| Usage | p-Orcacetophenone is an acetophenone derivative used in the preparation of sodium glucose co-transporter 2 inhibitors as antidiabetic agents. |
| 3,5-DIHYDROXY-4-ACETYLTOLUENE Basic information |
| Product Name: | 3,5-DIHYDROXY-4-ACETYLTOLUENE |
| Synonyms: | 3,5-DIHYDROXY-4-ACETYLTOLUENE;2,6-DIHYDROXY-4'-METHYLACETOPHENONE;ETHANONE, 1-(2,6-DIHYDROXY-4-METHYLPHENYL)-;4-acetyl-3,5-dihydroxytoluene;4-ACETYL-3,5-DIHYDROXYTOLUENE,98.5+%;1-(2,6-Dihydroxy-4-methylphenyl)ethanone;p-Orcacetophenone;1-(2,6-dihydroxy-4-Methylphenyl)ethan-1-one |
| CAS: | 1634-34-0 |
| MF: | C9H10O3 |
| MW: | 166.17 |
| EINECS: | |
| Product Categories: | Alcohols and Derivatives;Carbonyl Compounds;Aromatic Acetophenones & Derivatives (substituted);Aromatics;Intermediates |
| Mol File: | 1634-34-0.mol |
|
|
|
| 3,5-DIHYDROXY-4-ACETYLTOLUENE Chemical Properties |
| CAS DataBase Reference | 1634-34-0(CAS DataBase Reference) |
| Safety Information |
| 3,5-DIHYDROXY-4-ACETYLTOLUENE Usage And Synthesis |
| Usage | p-Orcacetophenone is an acetophenone derivative used in the preparation of sodium glucose co-transporter 2 inhibitors as antidiabetic agents. |