4-Nitrobenzoyl chloride, 98%, Thermo Scientific Chemicals
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4-Nitrobenzoyl chloride, 98%, Thermo Scientific Chemicals
4-Nitrobenzoyl chloride, 98%, Thermo Scientific Chemicals
4-Nitrobenzoyl chloride, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-Nitrobenzoyl chloride, 98%, Thermo Scientific Chemicals

CAS: 122-04-3 | C7H4ClNO3 | 185.56 g/mol
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250 g
10 g
Catalog number ALFA12543.30
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250 g
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Chemical Identifiers
CAS87-69-4
IUPAC Name2,3-dihydroxybutanedioic acid
Molecular FormulaC4H6O6
InChI KeyFEWJPZIEWOKRBE-UHFFFAOYNA-N
SMILESOC(C(O)C(O)=O)C(O)=O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Colorless to white to almost white
Appearance (Form)Crystalline powder or crystals
Infrared spectrumConforms
Melting point168°C to 172°C
Loss on drying=<0.5 % (1 g, 105°C)
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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.
RUO – Research Use Only

General References:

  1. Reagent for the preparation of crystalline esters.
  2. 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.
  3. Skácel, J.; Budka, J.; Eigner, V.; Lhoták, P. Regioselective Friedel-Crafts acylation of calix[4]arenes. Tetrahedron 2015, 71 (13), 1959-1965.