| Identification | More | [Name]
3,5-Difluorobenzylamine | [CAS]
90390-27-5 | [Synonyms]
3,5-DIFLUOROBENZYLAMINE
RARECHEM AL BW 0274
Difluorobenzylamine6
3,5-Difluorobenzylamine,97%
AIDS-011115
3,5-Difluorobenzylamine 97%
(3,5-Difluorophenyl)methanamine | [Molecular Formula]
C7H7F2N | [MDL Number]
MFCD00061244 | [Molecular Weight]
143.13 | [MOL File]
90390-27-5.mol |
| Chemical Properties | Back Directory | [Appearance]
Clear yellow liquid | [Melting point ]
261-262 °C(Solv: N,N-dimethylformamide (68-12-2)) | [Boiling point ]
184 °C (lit.) | [density ]
1.21 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.491(lit.)
| [Fp ]
165 °F
| [storage temp. ]
2-8°C(protect from light) | [form ]
clear liquid | [pka]
8.54±0.10(Predicted) | [color ]
Colorless to Almost colorless | [Specific Gravity]
1.21 | [Sensitive ]
Air Sensitive | [BRN ]
3538436 | [InChIKey]
VJNGGOMRUHYAMC-UHFFFAOYSA-N | [CAS DataBase Reference]
90390-27-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S27:Take off immediately all contaminated clothing .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 2735 8/PG 2
| [WGK Germany ]
3
| [Hazard Note ]
Corrosive | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29214990 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear yellow liquid | [Uses]
3,5-Difluorobenzylamine (DFBA) has been used as a derivatization reagent in the following studies:
- Determination of epichlorohydrin (ECH) in water by GC/MS analysis in selected ion monitoring (SIM) mode.
- Analysis of the epoxides 1,2-epoxybutane, epichlorohydrin, and epifluorohydrin in water by GC/MS analysis.
- Estimation of ECH in water by on-line solid-phase extraction (SPE) coupled to liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS) using a triple quadrupole mass spectrometer.
| [Synthesis]
General procedure for the synthesis of 3,5-difluorobenzylamine from 3,5-difluorobenzonitrile: 3,5-difluorobenzonitrile (4 g, 28.8 mmol) was added to a nickel Nguyen Nai slurry pre-washed with methanol, which had been treated with ammonia (100 ml) saturated methanol solution. The reaction mixture was shaken under 50 psi hydrogen pressure for 1.5 hours. Upon completion of the reaction, the reaction mixture was filtered and the filtrate evaporated. The residue was dissolved in ethyl acetate and subsequently extracted with 3N hydrochloric acid solution. The acidic aqueous phase was alkalized with 50% sodium hydroxide solution and extracted again with ethyl acetate. The organic phases were combined and concentrated by drying with anhydrous sodium sulfate to give 3.0 g (74% yield) of 3,5-difluorobenzylamine, the product was a yellow oil, which needed to be stored under nitrogen protection. | [References]
[1] Organic Letters, 1999, vol. 1, # 2, p. 183 - 185
[2] Patent: US4835154, 1989, A
[3] Patent: EP323737, 1989, A1
[4] Journal of Medicinal Chemistry, 1990, vol. 33, # 2, p. 781 - 789
[5] Patent: US4707488, 1987, A |
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