10919

Fmoc isothiocyanate

≥98.0% (CHN)

• Sinónimos: 9-Fluorenylmethoxycarbonyl isothiocyanate, 9-Fluorenylmethyl isothiocyanatoformate
• Fórmula empírica (notación de Hill): C₁₆H₁₁NO₂S
• Número de CAS: 199915-38-3
• Peso molecular: 281.33
• Beilstein/REAXYS Number: 7930648
• MDL number: MFCD01861169
• UNSPSC Code: 12352005
• PubChem Substance ID: 57646854
• NACRES: NA.22

Propiedades

• assay: ≥85% (coupling to amines); ≥98.0% (CHN)
• solubility: ethanol: soluble
• fluorescence: λ_ex 264 nm; λ_em 313 nm
• application(s): peptide synthesis
• functional group: Fmoc
• storage temp.: −20°C
• SMILES string: O=C(OCC1c2ccccc2-c3ccccc13)N=C=S
• InChI: 1S/C16H11NO2S/c18-16(17-10-20)19-9-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15H,9H2
• InChI key: DHMYULZVFHHEHE-UHFFFAOYSA-N

Descripción

Application

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.

Other Notes

Reagent for the synthesis of substituted thioureas from amines

Información de seguridad

• pictograms: GHS05,GHS07
• signalword: Danger
• hcodes: H315,H318,H335
• pcodes: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves