3-Nitrobenzaldehyde, 99%, Thermo Scientific Chemicals
3-Nitrobenzaldehyde, 99%, Thermo Scientific Chemicals
3-Nitrobenzaldehyde, 99%, Thermo Scientific Chemicals
3-Nitrobenzaldehyde, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Nitrobenzaldehyde, 99%, Thermo Scientific Chemicals

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Catalog NumberQuantity
ALFA13594.30250 g
Catalog number ALFA13594.30
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Quantity:
250 g
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Chemical Identifiers
CAS75-47-8
IUPAC Nametriiodomethane
Molecular FormulaCHI3
InChI KeyOKJPEAGHQZHRQV-UHFFFAOYSA-N
SMILESIC(I)I
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Bright yellow to dark yellow
Appearance (Form)Crystalline powder
Infrared spectrumConforms
Melting point119°C to 122°C
Loss on drying=<0.5 % (24 h) (Over silicagel)
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3-Nitrobenzaldehyde is used in the synthesis of other organic compounds, ranging from pharmaceuticals to plastic additives and intermediate for the processing of perfume and flavoring compounds and in the preparation of certain aniline 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
3-Nitrobenzaldehyde is used in the synthesis of other organic compounds, ranging from pharmaceuticals to plastic additives and intermediate for the processing of perfume and flavoring compounds and in the preparation of certain aniline dyes.

Solubility
Slightly soluble in water.

Notes
Air Sensitive. Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only

General References:

  1. Nidhi Jain.; Anil Kumar.; Shive M.S. Chauhan. Metalloporphyrin and heteropoly acid catalyzed oxidation of Cdouble bond; length as m-dashNOH bonds in an ionic liquid: biomimetic models of nitric oxide synthase. Tetrahedron Letters. 2005, 46, (15), 2599-2602.
  2. Vijay Nair.; Rajeev S Menon.; A.U Vinod.; S Viji. A facile three-component reaction involving [4+1] cycloaddition leading to furan annulated heterocycles . Tetrahedron Letters. 2002, 43, (12), 2293-2295.