4-CHLORO-6-METHOXY-5-NITROPYRIMIDINE
- Product Name
- 4-CHLORO-6-METHOXY-5-NITROPYRIMIDINE
- CAS No.
- 52854-14-5
- Chemical Name
- 4-CHLORO-6-METHOXY-5-NITROPYRIMIDINE
- Synonyms
- NSC 73560;4-CHLORO-6-METHOXY-5-NITROPYRIMIDINE;Pyrimidine, 4-chloro-6-methoxy-5-nitro-
- CBNumber
- CB82446329
- Molecular Formula
- C5H4ClN3O3
- Formula Weight
- 189.56
- MOL File
- 52854-14-5.mol
4-CHLORO-6-METHOXY-5-NITROPYRIMIDINE Property
- Melting point:
- 66℃
- Boiling point:
- 343.1±37.0 °C(Predicted)
- Density
- 1.532±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- -4.87±0.26(Predicted)
- Appearance
- White to off-white 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.
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
- C374963
- Product name
- 4-chloro-6-methoxy-5-nitropyrimidine
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- HCH0133260
- Product name
- 4-CHLORO-6-METHOXY-5-NITROPYRIMIDINE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $505.97
- Updated
- 2021/12/16
- Product number
- UT02480
- Product name
- 4-Chloro-6-methoxy-5-nitropyrimidine
- Purity
- 97%
- Packaging
- 1g
- Price
- $538.33
- Updated
- 2021/12/16
- Product number
- CM167424
- Product name
- 4-chloro-6-methoxy-5-nitropyrimidine
- Purity
- 95%
- Packaging
- 5g
- Price
- $1262
- Updated
- 2021/12/16
- Product number
- CD11110259
- Product name
- 4-Chloro-6-methoxy-5-nitropyrimidine
- Purity
- 95+%
- Packaging
- 5g
- Price
- $1337
- Updated
- 2021/12/16
4-CHLORO-6-METHOXY-5-NITROPYRIMIDINE Chemical Properties,Usage,Production
Synthesis
4316-93-2
124-41-4
52854-14-5
Sodium methanolate (2.70 g, 50.0 mmol) was added batchwise to a stirred suspension of 4,6-dichloro-5-nitropyrimidine (4.85 g, 25.0 mmol) in methanol (90 ml) at 0 °C over 10 min. After addition, the reaction mixture was maintained at 0°C and continued to stir for 2 hours. After completion of the reaction, the precipitate was collected by filtration. The filtrate was concentrated to dryness and the resulting residue was suspended in isohexane and filtered again. The filtrate was concentrated and the residue was purified by rapid column chromatography on silica gel, using a 5% ethyl acetate solution in isohexane as eluent. The grades containing the target product were collected and concentrated to give 4-methoxy-5-nitro-6-chloropyrimidine (3.50 g, 74% yield) as a white solid.
References
[1] Patent: WO2004/41826, 2004, A1. Location in patent: Page 42
[2] Patent: EP2527344, 2012, A1. Location in patent: Page/Page column 34
[3] Patent: WO2012/160030, 2012, A1. Location in patent: Page/Page column 138-139
[4] Journal of Medicinal Chemistry, 1993, vol. 36, # 11, p. 1630 - 1640
4-CHLORO-6-METHOXY-5-NITROPYRIMIDINE Preparation Products And Raw materials
Raw materials
Preparation Products
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