ChemicalBook--->CAS DataBase List--->660432-43-9

660432-43-9

660432-43-9 Structure

660432-43-9 Structure
IdentificationBack Directory
[Name]

(2-fluoro-4-nitrophenyl)methanol
[CAS]

660432-43-9
[Synonyms]

(2-fluoro-4-nitrophenyl)methanol
2-Fluoro-4-nitrobenzylalcohol97%
Benzenemethanol, 2-fluoro-4-nitro-
2-Fluoro-4-nitrobenzyl alcohol 97%
2-Fluoro-4-nitrobenzyl alcohol, 97%
3-Fluoro-4-(hydroxymethyl)nitrobenzene, (2-Fluoro-4-nitrophenyl)methanol
[Molecular Formula]

C7H6FNO3
[MDL Number]

MFCD11110168
[MOL File]

660432-43-9.mol
[Molecular Weight]

171
Chemical PropertiesBack Directory
[Melting point ]

103-105℃
[Boiling point ]

319.9±27.0 °C(Predicted)
[density ]

1.434±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Solid
[pka]

13.14±0.10(Predicted)
[color ]

White to yellow
[CAS DataBase Reference]

660432-43-9
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HazardClass ]

IRRITANT
[HS Code ]

2906290090
Spectrum DetailBack Directory
[Spectrum Detail]

(2-fluoro-4-nitrophenyl)methanol(660432-43-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Fluoro-4-nitrobenzaldehyde

157701-72-9

(2-fluoro-4-nitrophenyl)methanol

660432-43-9

General procedure for the synthesis of 2-fluoro-4-nitrobenzyl alcohol from 2-fluoro-4-nitrobenzaldehyde: To a solution of 2-fluoro-4-nitrobenzaldehyde (1.0 g, 5.92 mmol) in methanol (10 mL) was slowly added sodium borohydride (814 mg, 22 mmol). The reaction mixture was stirred at room temperature for 15 min and then concentrated by rotary evaporator. The concentrated residue was subjected to liquid-liquid partitioning with ethyl acetate (100 mL) and saturated aqueous sodium chloride solution (100 mL). The combined organic phases were washed with saturated aqueous sodium chloride solution (100 mL x 2) and dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated to give the red solid product 2-fluoro-4-nitrobenzyl alcohol (1.0 g, 99% yield).

[References]

[1] Patent: TWI602818, 2017, B. Location in patent: Paragraph 0481; 0482
[2] Patent: WO2014/173289, 2014, A1. Location in patent: Paragraph 0479; 0481; 0482
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