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4-BROMO-3-NITRO-BENZALDEHYDE

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CAS:163596-75-6
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Products Intro: Product Name:4-Bromo-3-nitrobenzaldehyde
CAS:163596-75-6
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4-BROMO-3-NITRO-BENZALDEHYDE manufacturers

  • 4-BROMO-3-NITRO-BENZALDEHYDE
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  • $100.00 / 1KG
  • 2025-09-25
  • CAS:163596-75-6
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  • Purity: 99%
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4-BROMO-3-NITRO-BENZALDEHYDE Basic information
Product Name:4-BROMO-3-NITRO-BENZALDEHYDE
Synonyms:TIMTEC-BB SBB009829;4-BROMO-3-NITRO-BENZALDEHYDE;AKOS B028535;ART-CHEM-BB B028535;Benzaldehyde,4-broMo-3-nitro-;3 - Nitro -4- BroMobenzaldehyde;4-Bromo-3-nitrobenzaldehyde 97%;JR-14016, 4-Bromo-3-nitrobenzaldehyde, 97%
CAS:163596-75-6
MF:C7H4BrNO3
MW:230.02
EINECS:
Product Categories:Aldehydes;C7;Carbonyl Compounds
Mol File:163596-75-6.mol
4-BROMO-3-NITRO-BENZALDEHYDE Structure
4-BROMO-3-NITRO-BENZALDEHYDE Chemical Properties
Melting point 104-108 °C (lit.)
Boiling point 289.3±30.0 °C(Predicted)
density 1.781±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
color White to Light red to Green
λmax295nm(CH3CN)(lit.)
InChIInChI=1S/C7H4BrNO3/c8-6-2-1-5(4-10)3-7(6)9(11)12/h1-4H
InChIKeySAFSVELFSYQXOV-UHFFFAOYSA-N
SMILESC(=O)C1=CC=C(Br)C([N+]([O-])=O)=C1
CAS DataBase Reference163596-75-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-50-43-38-22
Safety Statements 26-36-61-45-36/37
RIDADR UN 3077 9 / PGIII
WGK Germany 3
HS Code 2913000090
Storage Class11 - Combustible Solids
Hazard ClassificationsAquatic Acute 1
Eye Irrit. 2
Skin Irrit. 2
Skin Sens. 1
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
4-BROMO-3-NITRO-BENZALDEHYDE Usage And Synthesis
Uses4-Bromo-3-nitrobenzaldehyde is a benzaldehyde derivative, mainly used as an intermediate component in organic synthesis. It can be used to prepare 4-Bromo-3-chlorobenzoic acid and other benzoic acid compounds.
Synthesis
4-Bromobenzaldehyde

1122-91-4

4-BROMO-3-NITRO-BENZALDEHYDE

163596-75-6

Step 1. Synthesis of 4-bromo-3-nitrobenzaldehyde: NaNO3 (5.48 g, 64.47 mmol, 1.19 eq.) was added to a 100 mL three-necked round-bottomed flask, followed by slow addition of 98% H2SO4 (60 mL). The reaction mixture was stirred continuously for 1.5 h at 10 °C. After that, 4-bromobenzaldehyde (10 g, 54.05 mmol, 1.00 eq.) was added to the reaction system and stirring was continued for 2 h at the same temperature. The reaction process was monitored by thin layer chromatography (TLC, unfolding agent ratio EtOAc:PE = 1:5). Upon completion of the reaction, 200 g of ice was added to the reaction mixture to quench the reaction. The resulting white solid product was collected by filtration and washed thoroughly with distilled water (3 x 200 mL) to yield 4-bromo-3-nitrobenzaldehyde (11.72 g, 94% yield).

References[1] Patent: US8080566, 2011, B1. Location in patent: Page/Page column 65
[2] Medicinal Chemistry Research, 2018, vol. 27, # 7, p. 1782 - 1791
[3] Recueil des Travaux Chimiques des Pays-Bas, 1926, vol. 45, p. 694
[4] Recueil des Travaux Chimiques des Pays-Bas, 1929, vol. 48, p. 1137
[5] Journal of the Chemical Society, 1927, p. 25
4-BROMO-3-NITRO-BENZALDEHYDE Preparation Products And Raw materials
Raw materials4-Bromobenzaldehyde
Preparation Products3,4-Dibromobenzaldehyde-->2-NITRO-BIPHENYL-4-CARBALDEHYDE
Tag:4-BROMO-3-NITRO-BENZALDEHYDE(163596-75-6) Related Product Information
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