cas: 164650-44-6 — see every product listed under this CAS number, including other names
Efinaconazole (CAS 164650-44-6) is a chemical reagent available from Chemat. Available pack sizes: on request, 25mg, 10mg, 100mg, 5mg, 10mM (in 1ml dmso), 50mg, 500mg. Offered by: Chemat Brand, Dr. Ehrenstorfer, GLPBio, Biosynth.
| brand | Chemat Brand |
|---|---|
| catalog number | AO-E0053.17 |
| cas | 164650-44-6 |
| size | on request |
| availability | In stock |
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| brand | size | price | |
|---|---|---|---|
| Chemat Brand | on request | price on request | |
| Chemat Brand | on request | price on request | |
| Dr. Ehrenstorfer | 25mg | price on request | |
| GLPBio | 10mg | 760.86 Pln | |
| GLPBio | 100mg | 1757.80 Pln | |
| GLPBio | 5mg | 657.89 Pln | |
| GLPBio | 10mM (in 1ml dmso) | 1720.36 Pln | |
| GLPBio | 50mg | 1369.32 Pln | |
| Biosynth | 500mg | price on request | |
| Biosynth | 250mg | price on request | |
| Biosynth | 1000mg | price on request | |
| Biosynth | 2000mg | price on request | |
| Biosynth | 5000mg | price on request |
| delivery time | To be confirmed by Chemat |
|---|---|
| purity | No data |
Efinaconazole is a member of the class of triazoles that is butan-2-ol which is substituted at positions 1, 2, and 3 by 1,2,4-triazol-1-yl, 2,4-difluorophenyl, and 4-methylenepiperidin-1-yl groups, respectively (the 2R,3R stereoisomer). It is an antifungal drug used for the topical treatment of onychomycosis (a nail infection caused mainly by dermatophytes). It has a role as an EC 1.14.13.70 (sterol 14alpha-demethylase) inhibitor. It is a member of piperidines, a tertiary alcohol, an organofluorine compound, a tertiary amino compound, an olefinic compound, a conazole antifungal drug and a triazole antifungal drug.
Source: ChEBI
| Molecular formula | C18H22F2N4O |
|---|---|
| Molecular weight | 348.4 g/mol |
| IUPAC name | (2R,3R)-2-(2,4-difluorophenyl)-3-(4-methylidenepiperidin-1-yl)-1-(1,2,4-triazol-1-yl)butan-2-ol |
| InChIKey | NFEZZTICAUWDHU-RDTXWAMCSA-N |
| SMILES | C[C@H]([C@](CN1C=NC=N1)(C2=C(C=C(C=C2)F)F)O)N3CCC(=C)CC3 |
Computed by PubChem (NCBI)