Search
元素の検索
構造の検索
Thermo Scientific Chemicals
1,1'-Thiocarbonyldi-2(1H)-pyridone, 95%
CAS: 102368-13-8 | C11H8N2O2S | 232.26 g/mol
化学物質識別子
CAS102368-13-8
IUPAC Name1-(2-oxo-1,2-dihydropyridine-1-carbothioyl)-1,2-dihydropyridin-2-one
Molecular FormulaC11H8N2O2S
InChI KeyKXMMNJQMGILZDB-UHFFFAOYSA-N
SMILESO=C1C=CC=CN1C(=S)N1C=CC=CC1=O
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Orange to red
Assay (HPLC)≥94.0%
Identification (FTIR)Conforms
Melting Point (clear melt)153.0-166.0?C
FormPowder
1,1'-Thiocarbonyldi-2(1H)-pyridone is used in the preparation of thio-analogs of thioureas, sulforaphane and 2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one. It is involved in the preparation of norbiotinamine and its reactive derivatives such as isothiocyanates.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1,1′-Thiocarbonyldi-2(1H)-pyridone is used in the preparation of thio-analogs of thioureas, sulforaphane and 2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one. It is involved in the preparation of norbiotinamine and its reactive derivatives such as isothiocyanates.
Notes
Incompatible with strong oxidizing agents. Store in a cool place.
1,1′-Thiocarbonyldi-2(1H)-pyridone is used in the preparation of thio-analogs of thioureas, sulforaphane and 2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one. It is involved in the preparation of norbiotinamine and its reactive derivatives such as isothiocyanates.
Notes
Incompatible with strong oxidizing agents. Store in a cool place.
RUO – Research Use Only
General References:
- Kumar, S.; Spano, M. N.; Arya, D. P. Influence of linker length in shape recognition of B∗ DNA by dimeric aminoglycosides. Bioorg. Med. Chem. 2015, 23 (13), 3105-3109.
- Kim, M. S.; Ki, Y.; Ahn, S. Y.; Yoon, S.; Kim, S. E.; Park, H. G.; Sun, W.; Son, K.; Cui, M.; Choi, S.; Pearce, L. V.; Esch, T. E.; DeAndrea-Lazarus, I. A.; Blumberg, P. M.; Pearce, L. V. Asymmetric synthesis and receptor activity of chiral simplified resiniferatoxin (sRTX) analogues as transient receptor potential vanilloid 1 (TRPV1) ligands. Bioorg. Med. Chem. Lett. 2014, 24 (1), 382-385.