10919
Fmoc isothiocyanate
≥98.0% (CHN)
Synonym(s):
9-Fluorenylmethoxycarbonyl isothiocyanate, 9-Fluorenylmethyl isothiocyanatoformate
About This Item
Recommended Products
Assay
≥85% (coupling to amines)
≥98.0% (CHN)
solubility
ethanol: soluble
fluorescence
λex 264 nm; λem 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
Application
- 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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service