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Thermo Scientific Chemicals
4-Nitrobenzoyl chloride, 98%
CAS: 122-04-3 | C7H4ClNO3 | 185.56 g/mol
化学物質識別子
CAS122-04-3
IUPAC Name4-nitrobenzoyl chloride
Molecular FormulaC7H4ClNO3
InChI KeySKDHHIUENRGTHK-UHFFFAOYSA-N
SMILES[O-][N+](=O)C1=CC=C(C=C1)C(Cl)=O
さらに表示
仕様
スペックシート
スペックシートAssay (GC)≥97.5%
Identification (FTIR)Conforms
Melting Point (clear melt)70-75°C
Appearance (Color)Pale yellow to yellow
FormCrystalline powder or crystals or flakes or fused solid
4-Nitrobenzoyl chloride is used in the preparation of polysubstituted furanonaphthoquinoines. It is also involved in Michael addition, Henry reaction, O-alkylation and cycloaddition reactions. Further, it is employed as an intermediate in active pharmaceutical ingredient and dyes.
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
4-Nitrobenzoyl chloride is used in the preparation of polysubstituted furanonaphthoquinoines. It is also involved in Michael addition, Henry reaction, O-alkylation and cycloaddition reactions. Further, it is employed as an intermediate in active pharmaceutical ingredient and dyes.
Solubility
Soluble in terahydrofuran, dichloromethane, chloroform and pyridine.
Notes
Moisture sensitive. Incompatible with water, alcohols, oxidizing agents and strong bases.
4-Nitrobenzoyl chloride is used in the preparation of polysubstituted furanonaphthoquinoines. It is also involved in Michael addition, Henry reaction, O-alkylation and cycloaddition reactions. Further, it is employed as an intermediate in active pharmaceutical ingredient and dyes.
Solubility
Soluble in terahydrofuran, dichloromethane, chloroform and pyridine.
Notes
Moisture sensitive. Incompatible with water, alcohols, oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Reagent for the preparation of crystalline esters.
- Chen, W.; Feng, Y.; Zhang, M.; Wu, J.; Zhang, J.; Gao, X.; He, J.; Zhang, J. Homogeneous benzoylation of cellulose in 1-allyl-3-methylimidazolium chloride: Hammett correlation, mechanism and regioselectivity. RSC Adv. 2015, 5 (72), 58536-58542.
- Skácel, J.; Budka, J.; Eigner, V.; Lhoták, P. Regioselective Friedel-Crafts acylation of calix[4]arenes. Tetrahedron 2015, 71 (13), 1959-1965.