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Home > Encyclopedia > 2,3-Difluoroaniline

2,3-Difluoroaniline

2,3-Difluoroaniline structure

2,3-Difluoroaniline 

structure
  • CAS No:

    4519-40-8

  • Formula:

    C6H5F2N

  • Chemical Name:

    2,3-Difluoroaniline

  • Synonyms:

    Benzenamine,2,3-difluoro-;Aniline,2,3-difluoro-;2,3-Difluorobenzenamine;2,3-Difluoroaniline;2,3-Difluorophenylamine

  • Categories:

    Organic Chemistry  >  Organic Fluorine Compound

Description

clear light orange liquid

2,3-Difluoroaniline Basic Attributes

129.11

129.11

2716500

224-847-2

DTXSID80196415

2921420090

Characteristics

26

1.4

Clear light orange Liquid

1.3±0.1 g/cm3

69 °C @ Press: 12 Torr

160 °F

1.521

Keep away from heat, sparks, and flame. Keep away from sources of ignition. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Safety Information

III

6.1

2941

3

20/21/22-36/37/38

26-27-28-36/37/39-36

Xn,Xi

Irritant

P261-P280-P305 + P351 + P338

H302 + H312 + H332-H315-H319-H335

|Danger|H302 (95.65%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P311, P312, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 46 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2,3-Difluoroaniline Use and Manufacturing

Methods of Manufacturing

First, 0.638 g (2.01 mmol) of 1, 2-dibromo-4, 5-difluoro-3-nitrobenzene was dissolved in 4 mL of methanol, and then 48.4 mg of 10percent Pd/C (50percent wet) and 6.2 mg (0.06 mmol) of triethylamine were added. The atmosphere inside the reaction vessel was substituted with hydrogen, and the reaction mixture was reacted at 50°C for 2 hours under slight hydrogen pressurization. Analysis of the resulting reaction product by HPLC revealed 2.2 areapercent of 2, 3-dibromo-5, 6-difluoroaniline as a residual intermediate. Reaction was continued under the same conditions for a further 0.5 hours. The catalyst was then removed by filtration. The resulting liquid was subjected to quantitative analysis by HPLC. The yield of 2, 3-difluoroaniline was 93percent. The intermediate 2, 3-dibromo-5, 6-difluoroaniline had been eliminated.

Uses

intermediate for liquid crystal and drugs

Computed Properties

Molecular Weight:129.11
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Exact Mass:129.03900549
Monoisotopic Mass:129.03900549
Topological Polar Surface Area:26
Heavy Atom Count:9
Complexity:97.1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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