ChemicalBook > CAS DataBase List > 4-Chloro-2-Methoxy-3-nitropyridine

4-Chloro-2-Methoxy-3-nitropyridine

Product Name
4-Chloro-2-Methoxy-3-nitropyridine
CAS No.
934180-48-0
Chemical Name
4-Chloro-2-Methoxy-3-nitropyridine
Synonyms
4-Chloro-2-Methoxy-3-nitropyridine;Pyridine, 4-chloro-2-methoxy-3-nitro-
CBNumber
CB72707647
Molecular Formula
C6H5ClN2O3
Formula Weight
188.57
MOL File
934180-48-0.mol
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4-Chloro-2-Methoxy-3-nitropyridine Property

Boiling point:
276.0±35.0 °C(Predicted)
Density 
1.445±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
1.04±0.10(Predicted)
form 
solid
color 
Off-white
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Safety

HS Code 
2933399990
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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.

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N-Bromosuccinimide Price

TRC
Product number
C632228
Product name
4-Chloro-2-methoxy-3-nitropyridine
Packaging
10mg
Price
$45
Updated
2021/12/16
SynQuest Laboratories
Product number
4H54-5-3P
Product name
4-Chloro-2-methoxy-3-nitropyridine
Purity
97%
Packaging
250mg
Price
$258
Updated
2021/12/16
AK Scientific
Product number
5828DN
Product name
4-Chloro-2-methoxy-3-nitropyridine
Packaging
1g
Price
$745
Updated
2021/12/16
Chemcia Scientific
Product number
AA10-1309
Product name
4-Chloro-2-methoxy-3-nitro-pyridine
Purity
95%
Packaging
1g
Price
$475
Updated
2021/12/16
Crysdot
Product number
CD11010004
Product name
4-Chloro-2-methoxy-3-nitropyridine
Purity
95+%
Packaging
1g
Price
$503
Updated
2021/12/16
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4-Chloro-2-Methoxy-3-nitropyridine Chemical Properties,Usage,Production

Synthesis

165547-79-5

74-88-4

934180-48-0

The general procedure for the synthesis of 4-chloro-2-methoxy-3-nitropyridine from 2-hydroxy-3-nitro-4-chloropyridine and iodomethane was as follows: iodomethane (2.06 mL, 32.99 mmol) was slowly added to a suspension of 4-chloro-2-hydroxy-3-nitropyridine (2.87 g, 16.49 mmol) (for preparation, see Bioorg. Med. . chem. lett., 2003, 13, 125). The reaction mixture was heated with stirring at 85°C for 3.5 hours. Subsequently, a solution of sodium carbonate (16.49 mmol) in toluene (100 mL) was added to the reaction system and heating was continued. After the reaction mixture was cooled to room temperature, it was filtered through a diatomaceous earth pad and the solids were washed with toluene. The filtrate and washings were combined and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography using ethyl acetate:heptane (1:9, v/v) as eluent. The target fraction was collected and concentrated under reduced pressure to give the white solid product 4-chloro-2-methoxy-3-nitropyridine (1.99 g, 64% yield). Product characterization data: MS (ESI) m/z: 189/191 ([M + H]+).

References

[1] Patent: WO2007/39563, 2007, A1. Location in patent: Page/Page column 24
[2] Patent: US2007/112019, 2007, A1. Location in patent: Page/Page column 12/2

4-Chloro-2-Methoxy-3-nitropyridine Preparation Products And Raw materials

Raw materials

Preparation Products

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4-Chloro-2-Methoxy-3-nitropyridine Suppliers

Chiba Pharmaceutical Science and technology Co, Ltd.
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571-89925085
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sales@amadischem.com
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China
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Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
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Nanjing Shizhou Biology Technology Co.,Ltd
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934180-48-0, 4-Chloro-2-Methoxy-3-nitropyridineRelated Search:


  • 4-Chloro-2-Methoxy-3-nitropyridine
  • Pyridine, 4-chloro-2-methoxy-3-nitro-
  • 934180-48-0