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3-nitro-N-acrylphenylamine

Product Name
3-nitro-N-acrylphenylamine
CAS No.
17090-15-2
Chemical Name
3-nitro-N-acrylphenylamine
Synonyms
Alflutinib Impurity 12;3-nitro-N-acrylphenylamine;N-(3-nitrophenyl)prop-2-enamide;2-Propenamide, N-(3-nitrophenyl)-;3-nitro-N-acrylphenylamine ISO 9001:2015 REACH
CBNumber
CB43037829
Molecular Formula
C9H8N2O3
Formula Weight
192.17
MOL File
17090-15-2.mol
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3-nitro-N-acrylphenylamine Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Off-white to yellow Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

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
N900790
Product name
N-(3-Nitrophenyl)Acrylamide
Packaging
500mg
Price
$75
Updated
2021/12/16
AK Scientific
Product number
3639AL
Product name
N-(3-Nitrophenyl)acrylamide
Packaging
250mg
Price
$84
Updated
2021/12/16
AK Scientific
Product number
3639AL
Product name
N-(3-Nitrophenyl)acrylamide
Packaging
5g
Price
$199
Updated
2021/12/16
AK Scientific
Product number
3639AL
Product name
N-(3-Nitrophenyl)acrylamide
Packaging
10g
Price
$281
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM1026353
Product name
N-(3-NITROPHENYL)PROP-2-ENAMIDE
Purity
95.00%
Packaging
5MG
Price
$503.91
Updated
2021/12/16
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3-nitro-N-acrylphenylamine Chemical Properties,Usage,Production

Synthesis

814-68-6

99-09-2

17090-15-2

1. 3-Nitroaniline (6.90 g, 50 mmol) was weighed in a 250 mL round bottom flask, dichloromethane (100 mL) was added as solvent and stirring was initiated. 2. The reaction system was cooled to -78 °C and diisopropylethylamine (12.92 g, 100 mmol) was subsequently added to the reaction system. 3. Acryloyl chloride (6.80 g, 75 mmol) was slowly added dropwise to the reaction system under stirring conditions. 4. 4. After the dropwise addition, the reaction mixture was gradually warmed up to room temperature and the reaction was continued with stirring for 2 hours. 5. After completion of the reaction, the solvent was removed by concentration under reduced pressure to give the crude product. 6. The crude product was purified using column chromatography with the eluent being petroleum ether/ethyl acetate (4:1, v/v). 7. The target component was collected and the solvent was removed under reduced pressure to afford N-(3-nitrophenyl)acrylamide (9.6 g, 80% yield) as a yellow solid.

References

[1] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 21, p. 5505 - 5512
[2] European Journal of Medicinal Chemistry, 2017, vol. 126, p. 444 - 455
[3] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 14, p. 4179 - 4186
[4] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 2, p. 765 - 772
[5] European Journal of Medicinal Chemistry, 2018, vol. 143, p. 1847 - 1857

3-nitro-N-acrylphenylamine Preparation Products And Raw materials

Raw materials

Preparation Products

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3-nitro-N-acrylphenylamine Suppliers

Adamas Reagent, Ltd.
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17090-15-2, 3-nitro-N-acrylphenylamineRelated Search:


  • 3-nitro-N-acrylphenylamine
  • N-(3-nitrophenyl)prop-2-enamide
  • 2-Propenamide, N-(3-nitrophenyl)-
  • 3-nitro-N-acrylphenylamine ISO 9001:2015 REACH
  • Alflutinib Impurity 12
  • 17090-15-2