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1-METHYL-5-NITRO-1H-INDOLE

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Products Intro: Product Name:1-Methyl-5-nitro-1H-indole
CAS:29906-67-0
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:1-methyl-5-nitro-1H-indole
CAS:29906-67-0
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CAS:29906-67-0
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Products Intro: Product Name:1-Methyl-5-nitro-1H-indole
CAS:29906-67-0
Purity:0.98 Package:100g ,250g, 1kg , 5kg
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Products Intro: Product Name:1-Methyl-5-nitro-1H-indole
CAS:29906-67-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-02948

1-METHYL-5-NITRO-1H-INDOLE manufacturers

1-METHYL-5-NITRO-1H-INDOLE Basic information
Product Name:1-METHYL-5-NITRO-1H-INDOLE
Synonyms:1-METHYL-5-NITRO-1H-INDOLE;1-Methyl-5-nitro-1H-indole ,97%;1H-Indole, 1-Methyl-5-nitro-;1-Methyl-5-Nitroindole
CAS:29906-67-0
MF:C9H8N2O2
MW:176.17
EINECS:1806241-263-5
Product Categories:Heterocycle-Indole series
Mol File:29906-67-0.mol
1-METHYL-5-NITRO-1H-INDOLE Structure
1-METHYL-5-NITRO-1H-INDOLE Chemical Properties
Melting point 167 °C
Boiling point 339.2±15.0 °C(Predicted)
density 1.29±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility Chloroform (Slightly), DMSO (Slightly)
form Solid
color Dark Yellow to Very Dark Yellow
InChIInChI=1S/C9H8N2O2/c1-10-5-4-7-6-8(11(12)13)2-3-9(7)10/h2-6H,1H3
InChIKeyPXBQSCHRKSBGKV-UHFFFAOYSA-N
SMILESN1(C)C2=C(C=C([N+]([O-])=O)C=C2)C=C1
Safety Information
Risk Statements 22-41
Safety Statements 26-39
HazardClass IRRITANT
HS Code 29349990
MSDS Information
1-METHYL-5-NITRO-1H-INDOLE Usage And Synthesis
Chemical PropertiesLight yellow solid
Uses1-Methyl-5-nitro-1H-indole is used as a reagent in the synthesis of the antiasthmatic drug Zafirlukast (Z125000).
Synthesis
5-Nitroindole

6146-52-7

Dimethyl carbonate

616-38-6

1-METHYL-5-NITRO-1H-INDOLE

29906-67-0

1-METHYL-4-NITRO-1H-INDOLE

91482-63-2

Example 14 Synthesis of 1-methyl-5-nitroindole. To a 500 mL three-necked flask equipped with a thermocouple, condenser tube, and constant pressure dropping funnel was added 5-nitroindole (20.0 g, 123 mmol), potassium carbonate (4.0 g, 29 mmol), N,N-dimethylformamide (80 mL), and dimethyl carbonate (22 mL, 261.4 mmol). The reaction mixture was heated to reflux. The reaction progress was monitored by high performance liquid chromatography (HPLC) or thin layer chromatography (TLC) (unfolding agent: heptane solution of 30% ethyl acetate). After 3 hours of refluxing, complete conversion of 5-nitroindole was confirmed by the analytical method described above. The reaction mixture was then cooled to 10±5°C and diluted with water (160 mL), at which point a yellow precipitate was generated. The mixture was continued to be stirred at room temperature for 2 h, after which the solid product was collected by filtration, washed with water (100 mL), and finally dried under high vacuum at 60-65 °C for 24 h. 1-methyl-5-nitroindole (21.1 g, 97.1% yield) was obtained as a yellow solid.

References[1] Patent: US6326501, 2001, B1
1-METHYL-5-NITRO-1H-INDOLE Preparation Products And Raw materials
Preparation Products1H-Indol-5-amine, 1-methyl-N-2-propen-1-yl-
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