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

3-Nitrobenzaldehyde, 99%

CAS: 99-61-6 | C7H5NO3 | 151.121 g/mol
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Catalog NumberQuantity
ALFA13594.30250 g
Catalog number ALFA13594.30
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Quantity:
250 g
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Specifications
Chemical Name or Material3-Nitrobenzaldehyde
CAS99-61-6
Health Hazard 1H302-H315-H319-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
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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.