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Benzaldehyde, 2-methyl-4-nitro-

Product Name
Benzaldehyde, 2-methyl-4-nitro-
CAS No.
72005-84-6
Chemical Name
Benzaldehyde, 2-methyl-4-nitro-
Synonyms
2-Methyl-4-nitrobenzaldehyde;Benzaldehyde, 2-methyl-4-nitro-
CBNumber
CB51860545
Molecular Formula
C8H7NO3
Formula Weight
165.15
MOL File
72005-84-6.mol
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Benzaldehyde, 2-methyl-4-nitro- Property

Melting point:
69-70 °C
Boiling point:
321.1±30.0 °C(Predicted)
Density 
1.278±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to light yellow Solid
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Safety

HS Code 
2913000090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

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

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
B498265
Product name
2-methyl-4-nitrobenzaldehyde
Packaging
100mg
Price
$220
Updated
2021/12/16
AK Scientific
Product number
5585AJ
Product name
2-Methyl-4-nitrobenzaldehyde
Packaging
1g
Price
$237
Updated
2021/12/16
Apolloscientific
Product number
OR938627
Product name
2-Methyl-4-nitrobenzaldehyde
Purity
95%
Packaging
1g
Price
$464
Updated
2021/12/16
AK Scientific
Product number
5585AJ
Product name
2-Methyl-4-nitrobenzaldehyde
Packaging
5g
Price
$611
Updated
2021/12/16
Chemenu
Product number
CM254736
Product name
2-Methyl-4-nitrobenzaldehyde
Purity
95%
Packaging
10g
Price
$681
Updated
2021/12/16
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Benzaldehyde, 2-methyl-4-nitro- Chemical Properties,Usage,Production

Synthesis

89001-53-6

72005-84-6

The general procedure for the synthesis of 2-methyl-4-nitrobenzonitrile from 2-methyl-4-nitrobenzaldehyde was as follows: first, 2-methyl-4-nitrobenzonitrile (1 g, 6.17 mmol) was dissolved in anhydrous toluene (24.0 ml). Subsequently, the solution was cooled to 0 °C and a toluene solution of DIBAL-H (4.35 ml, 7.4 mmol) was added slowly and dropwise over a period of 10 min. The reaction mixture was stirred continuously at 0 °C for 2 hours. Upon completion of the reaction, the reaction was quenched by addition of 2N HCl (1 ml) at 0°C. After warming the mixture to room temperature, 2N HCl (1 ml) was added and sodium sulfate was added under vigorous stirring. The solid was removed by filtration and the solvent was evaporated to obtain the crude product. Finally, the crude product was purified by fast chromatography (using heptane/ethyl acetate as eluent) to give 2-methyl-4-nitrobenzaldehyde as an orange solid (0.68 g, 67% yield).

References

[1] Patent: WO2014/79850, 2014, A1. Location in patent: Page/Page column 54

Benzaldehyde, 2-methyl-4-nitro- Preparation Products And Raw materials

Raw materials

Preparation Products

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Benzaldehyde, 2-methyl-4-nitro- Suppliers

Shanghai Hanhong Scientific Co.,Ltd.
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72005-84-6, Benzaldehyde, 2-methyl-4-nitro-Related Search:


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