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2339-78-8

1,2-dichloro-4-fluoro-5-nitrobenzene

CAS: 2339-78-8

Molecular Formula: C6H2Cl2FNO2

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2339-78-8 - Names and Identifiers

Name 1,2-dichloro-4-fluoro-5-nitrobenzene
Synonyms 4,5-Dichloro-2-fluoronitrobenzene
1,2-DICHLORO-4-FLUORO-5-NITROBENZENE
1,2-dichloro-4-fluoro-5-nitrobenzene
3,4-Dichloro-2-fluoro-1-nitrobenzene
4-amino-5-fluoro-1-pentofuranosylpyrimidin-2(1H)-one
CAS 2339-78-8
InChI InChI=1/C9H12FN3O5/c10-3-1-13(9(17)12-7(3)11)8-6(16)5(15)4(2-14)18-8/h1,4-6,8,14-16H,2H2,(H2,11,12,17)

2339-78-8 - Physico-chemical Properties

Molecular FormulaC6H2Cl2FNO2
Molar Mass209.99
Density1.596 g/mL at 25 °C (lit.)
Melting Point17 °C (lit.)
Boling Point247 °C (lit.)
Flash Point>230°F
Vapor Presure1.34E-12mmHg at 25°C
AppearanceLow Melting Solid
ColorPale yellow
Storage ConditionSealed in dry,Room Temperature
Refractive Indexn20/D 1.575(lit.)

2339-78-8 - Risk and Safety

Risk CodesR20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37/39 - Wear suitable gloves and eye/face protection
WGK Germany3
Hazard NoteIrritant

2339-78-8 - Reference Information

Use 1, 2-dichloro-4-fluoro-5-nitrobenzene is also called 2-fluoro-4, 5-dichloronitrobenzene As an important pharmaceutical and pesticide intermediate, it has a wide range of uses. For example, 1) dibenzocycloheptene derivatives can be synthesized, which can treat neurological disorders; 2) benzenesulfonamide and benzimidazole derivatives with antibacterial properties; 3) quinazoline derivatives can effectively inhibit the activity of protein tyrosine kinase and reduce the incidence of cancer and diabetes; 4) pyrimidine carboxylic acid Derivatives, they are a broad-spectrum and efficient herbicide.
preparation acetylation and chlorination in one pot: add 22.2g of newly steamed p-fluoroaniline and 60 mL of glacial acetic acid to the reaction container, raise the temperature to 30 ℃, add 20.4g of acetic anhydride drop by drop under stirring. After acetic anhydride dripping, it is heated to 60~70 ℃, and the heat preservation reaction is over. Slightly cooling to 40 ℃, slowly introducing Cl2, maintaining the reaction temperature at 40~50 ℃, holding the reaction for 12 h, and the reaction is over. Pour the product into 500 mL of ice water, precipitate solid, filter, adjust the mother liquor to neutral with Na2CO3 and then filter to obtain crude product. The 60% ethanol aqueous solution was recrystallized to obtain 29.8g of white needle-like solid 2-chloro-4-fluoroacetanilide with a yield of 79.1%.
Last Update:2024-04-10 22:29:15
2339-78-8
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