2-CHLORO-3-NITROBENZALDEHYDE
- Product Name
- 2-CHLORO-3-NITROBENZALDEHYDE
- CAS No.
- 58755-57-0
- Chemical Name
- 2-CHLORO-3-NITROBENZALDEHYDE
- Synonyms
- 2-CHLORO-3-NITROBENZALDEHYDE;2-CHLORO-3-NIRO BENZALDEHYDE;Benzaldehyde, 2-chloro-3-nitro-;2-Chloro-3-nitrobenzaldehyde 95%;2-chloro-3-nitrobenzaldehyde58755-57-0
- CBNumber
- CB8110260
- Molecular Formula
- C7H4ClNO3
- Formula Weight
- 185.56
- MOL File
- 58755-57-0.mol
2-CHLORO-3-NITROBENZALDEHYDE Property
- Boiling point:
- 293.5±25.0 °C(Predicted)
- Density
- 1.485±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- powder
- color
- Yellow
Safety
- HS Code
- 2913000090
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
- C611595
- Product name
- 2-Chloro-3-nitrobenzaldehyde
- Packaging
- 250mg
- Price
- $65
- Updated
- 2021/12/16
- Product number
- FC139771
- Product name
- 2-Chloro-3-nitrobenzaldehyde
- Packaging
- 1g
- Price
- $67
- Updated
- 2021/12/16
- Product number
- W7175
- Product name
- 2-Chloro-3-nitrobenzaldehyde
- Packaging
- 100mg
- Price
- $72
- Updated
- 2021/12/16
- Product number
- W7175
- Product name
- 2-Chloro-3-nitrobenzaldehyde
- Packaging
- 1g
- Price
- $109
- Updated
- 2021/12/16
- Product number
- FC139771
- Product name
- 2-Chloro-3-nitrobenzaldehyde
- Packaging
- 2g
- Price
- $117
- Updated
- 2021/12/16
2-CHLORO-3-NITROBENZALDEHYDE Chemical Properties,Usage,Production
Synthesis
89639-98-5
58755-57-0
Step 2. Synthesis of 2-chloro-3-nitrobenzaldehyde: To a 250 mL three-necked round-bottomed flask, a solution of oxalyl chloride (5.42 g, 42.70 mmol, 1.10 eq.) in dichloromethane (DCM, 100 mL) was added. Subsequently, a solution of dimethyl sulfoxide (DMSO, 6.65 g, 85.11 mmol, 2.20 eq.) in DCM (15 mL) was added dropwise and the reaction system was kept at -78 °C. At this temperature, a solution of (2-chloro-3-nitrophenyl)methanol (7.23 g, 38.54 mmol, 1.00 eq.) in DCM (35 mL) was slowly added and stirred continuously for 1 hour. Then, triethylamine (TEA, 30 mL) was added at the same temperature and stirring was continued for 1 hour. Upon completion of the reaction, the reaction was quenched with water and extracted with DCM (3 x 100 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated on a rotary evaporator. The residue was purified by silica gel column chromatography using petroleum ether (PE):ethyl acetate (EA) = 10:1 as eluent to afford 2-chloro-3-nitrobenzaldehyde (5.3 g, 74% yield) as a light yellow solid.
References
[1] Journal of Medicinal Chemistry, 1988, vol. 31, # 5, p. 936 - 944
[2] Patent: US2011/34450, 2011, A1. Location in patent: Page/Page column 101; 102
[3] Patent: US2003/225053, 2003, A1. Location in patent: Page 24
[4] Patent: US8080566, 2011, B1. Location in patent: Page/Page column 72
[5] Tetrahedron, 2000, vol. 56, # 2, p. 165 - 173
2-CHLORO-3-NITROBENZALDEHYDE Preparation Products And Raw materials
Raw materials
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