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119946

Sigma-Aldrich

对氟苯甲酰氯

98%

别名:

4-Fluorobenzoic acid chloride, p-Fluorobenzoyl chloride

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About This Item

线性分子式:
FC6H4COCl
CAS号:
403-43-0
分子量:
158.56
Beilstein:
386215
EC 号:
206-961-4
MDL编号:
MFCD00000684
UNSPSC代码:
12352100
PubChem化学物质编号:
24847304
NACRES:
NA.22

质量水平

200

方案

98%

折射率

n20/D 1.532 (lit.)

沸点

82 °C/20 mmHg (lit.)

mp

10-12 °C (lit.)

密度

1.342 g/mL at 25 °C (lit.)

官能团

acyl chloride
fluoro

SMILES字符串

Fc1ccc(cc1)C(Cl)=O

InChI

1S/C7H4ClFO/c8-7(10)5-1-3-6(9)4-2-5/h1-4H

InChI key

CZKLEJHVLCMVQR-UHFFFAOYSA-N

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相关类别

一般描述

4-氟苯甲酰氯可与2,6-二甲基萘进行Friedel-Crafts酰化反应得到1,5-双（4-氟苯甲酰基）-2,6-二甲基萘。

象形图

Corrosion
GHS05

警示用语：

Danger

危险声明

H314

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

179.6 °F - closed cup

闪点(°C)

82 °C - closed cup

个人防护装备

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
WXBF2731V
WXBF0510V
WXBF1834V
WXBD6911V
WXBD5836V

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Solid-phase Friedel-Crafts acylation on polystyrene resins-synthesis of antiepiletic 1-aryl-3, 5-dihydro-4H-2, 3-benzodiazepin-4-ones.
Bevacqua F, et al.
Tetrahedron Letters, 42(43), 7683-7685 (2001)
Synthesis of a novel naphthalene-based poly (arylene ether-ketone) by polycondensation of 1, 5-bis (4-fluorobenzoyl)-2, 6-dimethylnaphthalene with bisphenol A.
Ohno M, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 33(15), 2647-2655 (1995)
Synthesis of [18F] GBR 12909, a dopamine reuptake inhibitor.
Haka MS and Kilbourn MR.
Journal of Labelled Compounds & Radiopharmaceuticals, 28(7), 793-799 (1990)
New multiblock copolymers of sulfonated poly (4'-phenyl-2, 5-benzophenone) and poly (arylene ether sulfone) for proton exchange membranes. II.
Ghassemi H, et al.
Polymer, 45(17), 5855-5862 (2004)
Novel electroactive aromatic polyamide with oligoanilines and azo groups in the backbone: synthesis, characterization and dielectric properties.
He L, et al.
Journal of Polymer Research, 19(1), 1-9 (2012)
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Friedel–Crafts Acylation

Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.

Friedel–Crafts Acylation

Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.

Friedel–Crafts Acylation

Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.

Friedel–Crafts Acylation

Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.

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