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2-BroMo-3-nitrobenzaldehyde

Product Name
2-BroMo-3-nitrobenzaldehyde
CAS No.
90407-21-9
Chemical Name
2-BroMo-3-nitrobenzaldehyde
Synonyms
2-BroMo-3-nitrobenzaldehyde;Benzaldehyde, 2-bromo-3-nitro-
CBNumber
CB22614786
Molecular Formula
C7H4BrNO3
Formula Weight
230.02
MOL File
90407-21-9.mol
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2-BroMo-3-nitrobenzaldehyde Property

Boiling point:
276.9±25.0 °C(Predicted)
Density 
1.781±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
color 
Light yellow to brown
InChI
InChI=1S/C7H4BrNO3/c8-7-5(4-10)2-1-3-6(7)9(11)12/h1-4H
InChIKey
ZAYPDOMLBUBLDN-UHFFFAOYSA-N
SMILES
C(=O)C1=CC=CC([N+]([O-])=O)=C1Br
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Safety

HS Code 
2913000090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

H400Very toxic to aquatic life

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

TRC
Product number
B699090
Product name
2-Bromo-3-nitrobenzaldehyde
Packaging
100mg
Price
$45
Updated
2021/12/16
TRC
Product number
B699090
Product name
2-Bromo-3-nitrobenzaldehyde
Packaging
500mg
Price
$65
Updated
2021/12/16
TRC
Product number
B699090
Product name
2-Bromo-3-nitrobenzaldehyde
Packaging
1g
Price
$75
Updated
2021/12/16
Usbiological
Product number
415795
Product name
2-Bromo-3-nitrobenzaldehyde
Packaging
100mg
Price
$305
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB74903
Product name
2-Bromo-3-nitrobenzaldehyde
Packaging
1g
Price
$160
Updated
2021/12/16
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2-BroMo-3-nitrobenzaldehyde Chemical Properties,Usage,Production

Synthesis

41085-43-2

90407-21-9

General procedure for the synthesis of 2-bromo-3-nitrobenzaldehyde using 2-bromo-3-nitrotoluene as starting material: first, chromium(VI) oxide (1.86 g, 6.94 mmol, 2.7 eq.) was dissolved in acetic anhydride (30 mL), and the solid was stirred until completely dissolved. Simultaneously, 2-bromo-3-nitrotoluene (1.5 g, 18.7 mmol, 1 eq.) was suspended in acetic anhydride (12 mL). Subsequently, sulfuric acid was slowly added dropwise to the suspension at 0 °C. Next, a previously prepared solution of chromium (VI) oxide was added dropwise over 1 hour and 30 minutes at the same temperature. After completion of the reaction, the mixture was warmed up to room temperature and stirred continuously for 3 hours. The reaction solution was neutralized in a small amount of ice water and the resulting solid product, 2-bromo-3-nitrobenzaldehyde (0.63 g, 39% yield) was collected by filtration, which could be used in subsequent steps without further purification. The product was characterized as follows: melting point 92 °C; IR spectra (KBr) υ 1697, 1539, 1519 cm-1; 1H NMR (DMSO-d6, 300 MHz) δ 14.24 (s, 1H), 8.26 (d, J = 7.8 Hz, 1H), 8.07 (d, J = 7.8 Hz, 1H), 7.79 (t, J = 8.1 Hz, 1H). Calculated elemental analysis (C7H4BrNO3): C, 36.55; H, 1.75; Br, 34.74; N, 6.09. Measured values: C, 36.60; H, 1.74; Br, 34.81; N, 6.04.

References

[1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 1, p. 1 - 10

2-BroMo-3-nitrobenzaldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

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2-BroMo-3-nitrobenzaldehyde Suppliers

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90407-21-9, 2-BroMo-3-nitrobenzaldehydeRelated Search:


  • 2-BroMo-3-nitrobenzaldehyde
  • Benzaldehyde, 2-bromo-3-nitro-
  • 90407-21-9