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Key Documents

196649

Sigma-Aldrich

邻氟苯腈

98%

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About This Item

線性公式:
FC6H4CN
CAS號碼:
分子量::
121.11
Beilstein:
2042184
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

98%

形狀

liquid

折射率

n20/D 1.505 (lit.)

bp

90 °C/21 mmHg (lit.)

密度

1.116 g/mL at 25 °C (lit.)

官能基

fluoro
nitrile

SMILES 字串

Fc1ccccc1C#N

InChI

1S/C7H4FN/c8-7-4-2-1-3-6(7)5-9/h1-4H

InChI 密鑰

GDHXJNRAJRCGMX-UHFFFAOYSA-N

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一般說明

2-Fluorobenzonitrile reacts with lithium N,N-dialkylaminoborohydride reagent to yield 2-(N,N-dialkylamino)benzylamines.

應用

2-Fluorobenzonitrile was used in the synthesis of :
  • 3-amino-1,2-benzisoxazoles
  • 6-(acetylaminomethyl)-3-amino-1,2-benzisoxazole
  • 5-(4′-methyl [1, 1′-biphenyl]-2-yl)-1H-tetrazole
  • xanthone-iminium triflates

象形圖

CorrosionExclamation mark

訊號詞

Danger

危險分類

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

165.2 °F - closed cup

閃點(°C)

74 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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H M Colquhoun et al.
Organic letters, 3(15), 2337-2340 (2001-07-21)
[reaction: see text] Condensation of 2-fluorobenzonitriles with phenoxides affords 2-aryloxybenzonitriles that cyclize cleanly in trifluoromethanesulfonic acid at room temperature to give xanthone-iminium triflates. The C=N bond in these compounds is remarkably resistant to hydrolysis, but prolonged reaction with strong aqueous
S Thomas et al.
The Journal of organic chemistry, 66(6), 1999-2004 (2001-04-13)
A novel tandem amination-reduction reaction has been developed in which 2-(N,N-dialkylamino)benzylamines are generated from 2-halobenzonitriles and lithium N,N-dialkylaminoborohydride (LAB) reagents. These reactions are believed to occur through a tandem S(N)Ar amination-reduction mechanism wherein the LAB reagent promotes halide displacement by
S D Lepore et al.
The Journal of organic chemistry, 65(10), 2924-2932 (2000-05-18)
Further exploration of the scope of our solid-phase method for the synthesis of 3-aminobenzisoxazoles (using the Kaiser oxime resin 1) is described. The effects of base, leaving group, and solvent on the nucleophilic aromatic substitution based resin-loading reaction are discussed.
Efficient synthesis of 5-(4'-methyl [1, 1'-biphenyl]-2-yl)-1H-tetrazole.
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The Journal of Organic Chemistry, 58(18), 5023-5024 (1993)
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