ALPHA-CHLORO-4-NITROBENZALDOXIME
- Product Name
- ALPHA-CHLORO-4-NITROBENZALDOXIME
- CAS No.
- 1011-84-3
- Chemical Name
- ALPHA-CHLORO-4-NITROBENZALDOXIME
- Synonyms
- -Chloro-4-nitrobenzaldoxime;a-Chloro-4-nitrobenzaldoxime;P-NITROBENZOHYDROXIMOYL CHLORIDE;4-nitrobenzohydroximoyl chloride;ALPHA-CHLORO-4-NITROBENZALDOXIME;N-hydroxy-4-nitrobenziMidoyl chloride;Benzenecarboximidoyl chloride, N-hydroxy-4-nitro-
- CBNumber
- CB8219989
- Molecular Formula
- C7H5ClN2O3
- Formula Weight
- 200.58
- MOL File
- 1011-84-3.mol
ALPHA-CHLORO-4-NITROBENZALDOXIME Property
- Melting point:
- 66-67 °C
- Boiling point:
- 376.6±44.0 °C(Predicted)
- Density
- 1.50±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 9.73±0.70(Predicted)
- Appearance
- Light yellow to yellow Solid
N-Bromosuccinimide Price
- Product number
- H1820
- Product name
- N-Hydroxy-4-nitrobenzimidoyl Chloride
- Purity
- min. 95.0 %
- Packaging
- 5G
- Price
- $185
- Updated
- 2025/07/31
- Product number
- H1820
- Product name
- N-Hydroxy-4-nitrobenzimidoyl Chloride
- Purity
- min. 95.0 %
- Packaging
- 25G
- Price
- $555
- Updated
- 2025/07/31
- Product number
- H539260
- Product name
- N-Hydroxy-4-nitrobenzimidoylChloride
- Packaging
- 100mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- H539260
- Product name
- N-Hydroxy-4-nitrobenzimidoylChloride
- Packaging
- 500mg
- Price
- $75
- Updated
- 2021/12/16
- Product number
- 9589AJ
- Product name
- alpha-Chloro-4-nitrobenzaldoxime
- Packaging
- 1g
- Price
- $89
- Updated
- 2021/12/16
ALPHA-CHLORO-4-NITROBENZALDOXIME Chemical Properties,Usage,Production
Synthesis Reference(s)
The Journal of Organic Chemistry, 36, p. 2146, 1971 DOI: 10.1021/jo00814a024
Synthesis
1129-37-9
1011-84-3
General procedure for the synthesis of 4-nitrochlorobenzaldehyde oxime from 4-nitrobenzaldoxime: 4-nitrobenzaldoxime (087 mg, 5.3 mmol) was dissolved in anhydrous dimethylformamide (4.6 mL) and the solution was cooled down to 0 °C. N-chlorosuccinimide (800 mg, 6.0 mmol) was added in batches with stirring. The cooling bath was removed and the resulting mixture was stirred at room temperature for 4 hours. After completion of the reaction, ice water (20 mL) was added and the resulting mixture was extracted with ether. The organic layer was washed three times with water, once with saturated brine and dried with anhydrous magnesium sulfate. The solvent was removed under reduced pressure after filtration to give a white solid 4-nitrochlorobenzaldehyde oxime (1.064 g, 100%).1H NMR (400 MHz, CDCl3) data were as follows: δ 8.37 (s, 1H, -OH), 8.27 (d, J = 8.8 Hz, 2H, Ar-H), 8.04 (d, J = 8.8 Hz, 2H, Ar-H).
References
[1] Patent: WO2011/15037, 2011, A1. Location in patent: Page/Page column 42; 53
[2] Patent: US2011/212975, 2011, A1. Location in patent: Page/Page column 14; 19
[3] Tetrahedron Letters, 2006, vol. 47, # 9, p. 1457 - 1460
[4] Journal of Chemical Research, 2007, # 1, p. 26 - 28
[5] Tetrahedron, 2000, vol. 56, # 8, p. 1057 - 1064
ALPHA-CHLORO-4-NITROBENZALDOXIME Preparation Products And Raw materials
Raw materials
Preparation Products
ALPHA-CHLORO-4-NITROBENZALDOXIME Suppliers
- Tel
- --
- Fax
- --
- interchim@interchim.com
- Country
- France
- ProdList
- 6302
- Advantage
- 76
View Lastest Price from ALPHA-CHLORO-4-NITROBENZALDOXIME manufacturers
- Product
- ALPHA-CHLORO-4-NITROBENZALDOXIME 1011-84-3
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 99.0%
- Supply Ability
- 1000KG
- Release date
- 2024-08-06