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103799

Sigma-Aldrich

五氟苯酚

≥99%, for peptide synthesis, ReagentPlus®

别名:

2,3,4,5,6-五氟苯酚

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About This Item

线性分子式:
C6F5OH
CAS号:
771-61-9
分子量:
184.06
Beilstein:
1912584
EC號碼:
212-235-8
MDL號碼:
MFCD00002156
分類程式碼代碼:
12352104
PubChem物質ID:
24846624
NACRES:
NA.22

产品名称

五氟苯酚, ReagentPlus®, ≥99%

品質等級

100

產品線

ReagentPlus®

化驗

≥99%

形狀

solid

bp

143 °C (lit.)

mp

34-36 °C (lit.)

應用

peptide synthesis

官能基

fluoro

SMILES 字串

Oc1c(F)c(F)c(F)c(F)c1F

InChI

1S/C6HF5O/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H

InChI 密鑰

XBNGYFFABRKICK-UHFFFAOYSA-N

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相关类别

一般說明

五氟苯酚被广泛用作溶液和固相肽合成的前体。 它也参与制备芳香族氟衍生物。.

應用

五氟苯酚可作为反应物与以下物质反应合成五氟苯基酯：
  • 在二环己基碳二亚胺和乙酸乙酯存在的情况下与N-保护氨基酸反应。在1-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐存在的情况下与
  • 叔-丁氧羰基-L-丙氨酰甘氨酸反应。
  • 在吡啶、二异丙基碳二亚胺和乙腈存在的情况下与脂肪族二羧酸反应。
它也可作为反应物用于合成五氟苯酚甲酸酯，其可用作有机合成中的甲酰化剂。

法律資訊

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H302 + H312

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

161.6 °F - closed cup

閃點（°C）

72 °C - closed cup

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000223225
STBK4816
0000128128
STBK0327
STBJ9928

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Pentafluorophenol
Jones K
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
M Adamczyk et al.
Bioconjugate chemistry, 8(2), 253-255 (1997-03-01)
A mixture of 5- and 6-carboxyfluorescein was activated with 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride in the presence of either N-hydroxysuccinimide or pentafluorophenol to give the corresponding succinimidyl and pentafluorophenyl esters. The regioisomeric mixtures were separated to give the 5- and 6-succinimidyl and pentafluorophenyl
Nadine Grebenstein et al.
Journal of chromatography. A, 1243, 39-46 (2012-05-09)
Of the eight natural vitamin E congeners (α-, β-, γ-, and δ-tocopherol and α-, β-, γ-, and δ-tocotrienol), the non-α-tocopherol congeners have unique biological properties that may contribute to human health. Their study in vivo has been complicated by the
Nicolas Abello et al.
Analytical chemistry, 80(23), 9171-9180 (2008-10-29)
Stable isotope labeling (SIL) in combination with liquid chromatography-mass spectrometry is one of the most widely used quantitative analytical methods due to its sensitivity and ability to deal with extremely complex biological samples. However, SIL methods for metabolite analysis are
Total synthesis and confirmation of the revised structures of azaspiracid-2 and azaspiracid-3.
K C Nicolaou et al.
Angewandte Chemie (International ed. in English), 45(16), 2609-2615 (2006-03-21)
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Separation of 2-Chlorophenol; 2,4-Dichlorophenol; 2,4,6-Tribromophenol; 2,4,6-Trichlorophenol; 2,4-Dinitrophenol; Pentafluorophenol; 2-Methylphenol, analytical standard; 2,3,4,6-Tetrachlorophenol; Pentachlorophenol; 4-Nitrophenol; 2-Bromophenol; 2,3,5,6-Tetrachlorophenol; 2,3,5-Trichlorophenol; 4-Chloro-3-methylphenol; 2,4,5-Trichlorophenol; 4-Methylphenol, analytical standard; 2,4-Dimethylphenol; 2-Nitrophenol; 3-Methylphenol, analytical standard; Phenol; 2-Methyl-4,6-dinitrophenol; 2,3,4-Trichlorophenol; 2,6-Dichlorophenol; 2,3,4,5-Tetrachlorophenol

US EPA Method 8041: GC Analysis of Phenols on Equity®-5

Separation of 2-Chlorophenol; 2,4-Dichlorophenol; 2,4,6-Tribromophenol; 2,4,6-Trichlorophenol; 2,4-Dinitrophenol; Pentafluorophenol; 2-Methylphenol, analytical standard; 2,3,4,6-Tetrachlorophenol; Pentachlorophenol; 4-Nitrophenol; 2-Bromophenol; 2,3,5,6-Tetrachlorophenol; 2,3,5-Trichlorophenol; 4-Chloro-3-methylphenol; 2,4,5-Trichlorophenol; 4-Methylphenol, analytical standard; 2,4-Dimethylphenol; 2-Nitrophenol; 3-Methylphenol, analytical standard; Phenol; 2-Methyl-4,6-dinitrophenol; 2,3,4-Trichlorophenol; 2,6-Dichlorophenol; 2,3,4,5-Tetrachlorophenol

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