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
3-nitro-N-acrylphenylamine Property
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- Off-white to yellow Solid
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.
N-Bromosuccinimide Price
- Product number
- N900790
- Product name
- N-(3-Nitrophenyl)Acrylamide
- Packaging
- 500mg
- Price
- $75
- Updated
- 2021/12/16
- Product number
- 3639AL
- Product name
- N-(3-Nitrophenyl)acrylamide
- Packaging
- 250mg
- Price
- $84
- Updated
- 2021/12/16
- Product number
- 3639AL
- Product name
- N-(3-Nitrophenyl)acrylamide
- Packaging
- 5g
- Price
- $199
- Updated
- 2021/12/16
- Product number
- 3639AL
- Product name
- N-(3-Nitrophenyl)acrylamide
- Packaging
- 10g
- Price
- $281
- Updated
- 2021/12/16
- Product number
- CHM1026353
- Product name
- N-(3-NITROPHENYL)PROP-2-ENAMIDE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $503.91
- Updated
- 2021/12/16
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
3-nitro-N-acrylphenylamine Suppliers
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