ChemicalBook--->CAS DataBase List--->5858-28-6

5858-28-6

5858-28-6 Structure

5858-28-6 Structure
IdentificationBack Directory
[Name]

5-METHYL-2-NITROBENZALDEHYDE
[CAS]

5858-28-6
[Synonyms]

5-METHYL-2-NITROBENZALDEHYDE
2-Nitro-5-methylbenzaldehyde
Benzaldehyde, 5-methyl-2-nitro-
[Molecular Formula]

C8H7NO3
[MDL Number]

MFCD08703362
[MOL File]

5858-28-6.mol
[Molecular Weight]

165.15
Chemical PropertiesBack Directory
[Melting point ]

64 °C
[Boiling point ]

314.0±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]

Light yellow to green yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2913000090
Spectrum DetailBack Directory
[Spectrum Detail]

5-METHYL-2-NITROBENZALDEHYDE(5858-28-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-METHYL-2-NITROBENZYL ALCOHOL

66424-92-8

5-METHYL-2-NITROBENZALDEHYDE

5858-28-6

General procedure for the synthesis of 5-methyl-2-nitrobenzaldehyde from 5-methyl-2-nitrobenzyl alcohol: a) 5-methyl-2-nitrobenzyl alcohol (10 g, 59.88 mmol) was dissolved in dichloromethane (210 mL). Subsequently 3A molecular sieves (54 g) and pyridinium dichromate (22.53 g, 59.88 mmol) were added. The reaction mixture was stirred at room temperature for 6 hours. After completion of the reaction, the crude product was filtered through a short silica gel column and concentrated under reduced pressure. The residue was purified by fast column chromatography (silica gel, 10-20% ethyl acetate/hexane as eluent) to afford 7.84 g (79% yield) of the target compound 5-methyl-2-nitrobenzaldehyde as a colorless oil.1H NMR (CDCl3) δ 10.41 (m, 1H), 8.02 (m, 1H), 7.69 (s, 1H), 7.53 (d, 1H). 1H), 2.51 (s, 3H).

[References]

[1] Patent: US2004/10004, 2004, A1. Location in patent: Page 22
[2] Journal of Organic Chemistry, 1980, vol. 45, # 7, p. 1334 - 1336
[3] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2001, vol. 40, # 5, p. 436 - 437
[4] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2001, vol. 40, # 4, p. 329 - 330
[5] Bulletin of the Korean Chemical Society, 2011, vol. 32, # 12, p. 4309 - 4315
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