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Merck

103713

Sigma-Aldrich

2,3,4,5,6-五氟苯胺

99%

别名:

Pentafluoroaniline

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About This Item

线性分子式:
C6F5NH2
CAS号:
分子量:
183.08
Beilstein:
1819387
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

99%

形狀

solid

bp

153 °C (lit.)

mp

33-35 °C (lit.)

溶解度

toluene: soluble

官能基

fluoro

SMILES 字串

Nc1c(F)c(F)c(F)c(F)c1F

InChI

1S/C6H2F5N/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H2

InChI 密鑰

NOXLGCOSAFGMDV-UHFFFAOYSA-N

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一般說明

2,3,4,5,6-五氟苯胺形成金属-药物复合物,顺-Pt-(2,3,4,5,6-五氟苯胺) 2 -Br 2 对抗杜氏利什曼原虫的前鞭毛体。

應用

2,3,4,5,6-五氟苯胺可用于制备三氟磷酸五氟苯胺,这是一种酯化和硫酯化的高效催化剂 。2,3,4,5,6-五氟苯胺用于合成了具有两个阴离子 [N,O] 双齿配体水杨醛亚胺的钛配合物

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

163.4 °F

閃點(°C)

73 °C

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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C M Mesa-Valle et al.
The Journal of antimicrobial chemotherapy, 40(1), 47-57 (1997-07-01)
The action of 16 newly synthesized metal complexes having the general structure cis-Pt-(II)-Xn-Ln have been tested in vitro against the promastigote forms of Leishmania donovani. The metal complexes at 24 h and maximum dosages inhibited growth from 0%, e.g. in
Bis (salicylaldiminato) titanium complexes containing bulky imine substituents: Synthesis, characterization and ethene polymerization studies.
Parssinen A, et al.
European Journal of Inorganic Chemistry, 2005(11), 2100-2109 (2005)
Pentafluorophenylammonium triflate (PFPAT): an efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation.
Funatomi T, et al.
Green Chemistry, 8(12), 1022-1027 (2006)
Vasily A Ilichev et al.
Dalton transactions (Cambridge, England : 2003), 48(3), 1060-1066 (2019-01-03)
To obtain new efficient lanthanide-based NIR luminophores perfluorinated 2-mercaptobenzothiazole was used as a ligand. The ate-complexes [(Ln(mbtF)4)-(Na(DME)3)+] of Nd (1), Sm (2), Tb (3), Er (4), Yb (5) and [(Y(mbtF)4)-(Li(DME)3)+] (6) were synthesized in high yields by the reactions of
I M Rietjens et al.
Chemico-biological interactions, 77(3), 263-281 (1991-01-01)
Metabolism and bioactivation of fluoroanilines was studied both in vitro in microsomal systems and in vivo. 4-Fluoroaniline and pentafluoroaniline and their non-para fluorinated analogues were used as the model compounds. Special attention was focussed on bioactivation to reactive benzoquinoneimines. Cytochrome

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