2-Methyl-5-nitrobenzaldehyde

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:2-Methyl-5-nitrobenzaldehyde
CAS:16634-91-6
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: career henan chemical co
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Products Intro: Product Name:2-Methyl-5-nitrobenzaldehyde
CAS:16634-91-6
Purity:99% Package:1KG;1USD
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:2-Methyl-5-nitrobenzaldehyde
CAS:16634-91-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-00654
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:2-methyl-5-nitrobenzaldehyde
CAS:16634-91-6
Purity:99% Package:1kg
Company Name: Fuxin Pharmaceutical
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Products Intro: Product Name:2-Methyl-5-nitrobenzaldehyde
CAS:16634-91-6
Purity:99% Package:1kg; 25kg; or larger package as required Remarks:pharmaceutical intermediates;Chemical Intermediate

2-Methyl-5-nitrobenzaldehyde manufacturers

2-Methyl-5-nitrobenzaldehyde Basic information
Product Name:2-Methyl-5-nitrobenzaldehyde
Synonyms:2-METHYL-5-NITROBENZALDEHYDE, 95+%;2-METHYL-5-NITROBENZALDEHYDE;Benzaldehyde, 2-methyl-5-nitro-;2,6-bis(trifluoroethoxy)aniline
CAS:16634-91-6
MF:C8H7NO3
MW:165.15
EINECS:
Product Categories:API intermediates;Aromatic Aldehydes & Derivatives (substituted)
Mol File:16634-91-6.mol
2-Methyl-5-nitrobenzaldehyde Structure
2-Methyl-5-nitrobenzaldehyde Chemical Properties
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 Information
HS Code 2913000090
MSDS Information
2-Methyl-5-nitrobenzaldehyde Usage And Synthesis
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
2-Methyl-5-nitrobenzaldehyde Preparation Products And Raw materials
Raw materials(2-METHYL-5-NITROPHENYL)METHANOL-->Pyridinium chlorochromate-->Dichloromethane
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