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ChemicalBook--->CAS DataBase List--->16634-91-6

16634-91-6

16634-91-6 Structure

16634-91-6 Structure
IdentificationBack Directory
[Name]

2-Methyl-5-nitrobenzaldehyde
[CAS]

16634-91-6
[Synonyms]

2-METHYL-5-NITROBENZALDEHYDE
Benzaldehyde, 2-methyl-5-nitro-
2-METHYL-5-NITROBENZALDEHYDE, 95+%
[Molecular Formula]

C8H7NO3
[MDL Number]

MFCD03840506
[MOL File]

16634-91-6.mol
[Molecular Weight]

165.15
Chemical PropertiesBack Directory
[Melting point ]

53.0 to 57.0 °C
[Boiling point ]

114°C/0.2mmHg(lit.)
[density ]

1.278±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

powder to crystal
[color ]

White to Light yellow to Light orange
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2913000090
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methyl-5-nitrobenzaldehyde(16634-91-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

(2-METHYL-5-NITROPHENYL)METHANOL

22474-47-1

2-Methyl-5-nitrobenzaldehyde

16634-91-6

General steps: 1. In a dry reaction flask, 2-methyl-5-nitrobenzyl alcohol (20 mmol) was dissolved in dichloromethane (DCM, 100 mL). 2. Pyridinium chlorochromate (PCC, 28-40 mmol) was added to the above solution. 3. The reaction mixture was heated to reflux (oil bath temperature was maintained at 55 °C) and the reaction lasted for 1-4 hours. 4. The progress of the reaction was monitored by thin layer chromatography (TLC) and/or liquid chromatography-mass spectrometry (LCMS) during the reaction. 5. Upon completion of the reaction, the mixture was cooled to room temperature. 6. post-processing, including isolation and purification of the product, is carried out according to the method described in variant B.

[References]

[1] Patent: US2015/218086, 2015, A1. Location in patent: Paragraph 0529; 0530; 0573
[2] Patent: WO2017/24009, 2017, A1. Location in patent: Paragraph 0560; 0592
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