1-(4-BROMOPHENYL)-2-NITROPROPENE
- Product Name
- 1-(4-BROMOPHENYL)-2-NITROPROPENE
- CAS No.
- 131981-75-4
- Chemical Name
- 1-(4-BROMOPHENYL)-2-NITROPROPENE
- Synonyms
- 1-(4-BROMOPHENYL)-2-NITROPROPENE;4'-BROMO-BETA-METHYL-BETA-NITROSTYRENE;1-Bromo-4-(2-nitroprop-1-en-1-yl)benzene;1-bromo-4-[(1E)-2-nitro-1-propenyl]benzene;(E)-1-bromo-4-(2-nitroprop-1-en-1-yl)benzene;1-bromo-4-[(1E)-2-nitroprop-1-en-1-yl]benzene;Benzene, 1-bromo-4-[(1E)-2-nitro-1-propen-1-yl]-
- CBNumber
- CB7200845
- Molecular Formula
- C9H8BrNO2
- Formula Weight
- 242.07
- MOL File
- 131981-75-4.mol
1-(4-BROMOPHENYL)-2-NITROPROPENE Property
- Melting point:
- 93-95 °C(Solv: methanol (67-56-1))
- Boiling point:
- 322.9±17.0 °C(Predicted)
- Density
- 1.520±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
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
- B703515
- Product name
- (E)-1-Bromo-4-(2-nitroprop-1-en-1-yl)benzene
- Packaging
- 25mg
- Price
- $75
- Updated
- 2021/12/16
- Product number
- HCH0123645
- Product name
- 1-(4-BROMOPHENYL)-2-NITROPROPENE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $496.14
- Updated
- 2021/12/16
- Product number
- A334577
- Product name
- (E)-1-Bromo-4-(2-nitroprop-1-en-1-yl)benzene
- Purity
- 97%
- Packaging
- 5g
- Price
- $232
- Updated
- 2021/12/16
- Product number
- 131981754
- Product name
- (E)-1-Bromo-4-(2-nitroprop-1-en-1-yl)benzene
- Packaging
- 5g
- Price
- $367.5
- Updated
- 2021/12/16
- Product number
- A334577
- Product name
- (E)-1-Bromo-4-(2-nitroprop-1-en-1-yl)benzene
- Purity
- 97%
- Packaging
- 100mg
- Price
- $18
- Updated
- 2021/12/16
1-(4-BROMOPHENYL)-2-NITROPROPENE Chemical Properties,Usage,Production
Synthesis
79-24-3
1122-91-4
131981-75-4
GENERAL METHOD: To a solution of p-bromobenzaldehyde (3.6 mmol) in glacial acetic acid (4 mL) was added nitroethane (7.2 mmol) followed by cyclohexylamine (3.6 mmol, 0.4 mL). The reaction mixture was placed in a microwave reactor and heated at 120 °C for 30 min. After completion of the reaction, it was cooled to room temperature, water (10 mL) was added to the reaction mixture and left to precipitate the product. The precipitated (E)-1-bromo-4-(2-nitroprop-1-en-1-yl)benzene was collected by filtration. The filtrate was further diluted with water (20 mL) and extracted with dichloromethane (3 x 10 mL). The organic phases were combined and washed with saturated aqueous NaHCO3 (3 x 10 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated in vacuum to remove the solvent to obtain the crude product. The crude product was purified by silica gel fast column chromatography (eluent: dichloromethane/hexane) and finally recrystallized with ethanol to obtain pure (E)-1-bromo-4-(2-nitroprop-1-en-1-yl)benzene.
References
[1] Tetrahedron, 2008, vol. 64, # 27, p. 6294 - 6299
[2] Tetrahedron Letters, 1986, vol. 27, # 33, p. 3843 - 3844
[3] Chemical Communications, 2016, vol. 52, # 65, p. 10060 - 10063
[4] Medicinal Chemistry, 2018, vol. 14, # 2, p. 181 - 199
[5] Patent: US6303816, 2001, B1
1-(4-BROMOPHENYL)-2-NITROPROPENE Preparation Products And Raw materials
Raw materials
Preparation Products
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