| Identification | Back Directory | [Name]
FMOC ISOTHIOCYANATE | [CAS]
199915-38-3 | [Synonyms]
Fmoc-isothiocyanate≥ 95% (NMR)
Fmoc isothiocyanate >=98.0% (CHN)
9-fluorenylmethoxycarbonyl isothiocyanate
9H-Fluoren-9-ylmethoxycarbonyl isothiocyanate
(9H-fluoren-9-yl)methyl N-carbothioylcarbamate
O-(9H-fluoren-9-yl)methyl carbonisothiocyanatidate
Carbon(isothiocyanatidic) acid 9H-fluoren-9-ylmethyl ester
9H-fluoren-9-ylmethyl N-(sulfanylidenemethylidene)carbamate
9-Fluorenylmethoxycarbonyl isothiocyanate, 9-Fluorenylmethyl isothiocyanatoformate | [Molecular Formula]
C16H11N1O2S1 | [MDL Number]
MFCD01861169 | [MOL File]
199915-38-3.mol | [Molecular Weight]
281.33 |
| Chemical Properties | Back Directory | [Melting point ]
42-46 °C
| [Boiling point ]
433.1±14.0 °C(Predicted) | [density ]
1.26 | [storage temp. ]
−20°C
| [solubility ]
ethanol: soluble
| [form ]
Liquid | [color ]
Clear yellow to brown | [BRN ]
7930648 |
| Hazard Information | Back Directory | [Chemical Properties]
Light yellow solid | [Uses]
Fmoc isothiocyanate can be used:
- As a starting material in the preparation of biologically relevant pharmacophores named N-aryl-N′-carboalkoxy guanidines.
- In one of the intermediate steps for the synthesis of N-aryl-N-thiazolyl derivatives.
- To synthesize cyclic isothiourea derivatives as potent neuropeptide Y (NPY) Y1?receptor antagonists.
- To prepare 2-aminothiazoles, aminobenz-imidazole conjugated thiazoles, and thiazole derived cyclopeptides.
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Sigma-Aldrich
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