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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號碼:
206-961-4
MDL號碼:
MFCD00000684
分類程式碼代碼:
12352100
PubChem物質ID:
24847304
NACRES:
NA.22

化驗

98%

折射率

n20/D 1.532 (lit.)

bp

82 °C/20 mmHg (lit.)

mp

10-12 °C (lit.)

密度

1.342 g/mL at 25 °C (lit.)

官能基

acyl chloride

SMILES 字串

Fc1ccc(cc1)C(Cl)=O

InChI

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

InChI 密鑰

CZKLEJHVLCMVQR-UHFFFAOYSA-N

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相关类别

一般說明

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。

象形圖

Corrosion
GHS05

訊號詞

Danger

危險聲明

H314

危險分類

Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類（WGK）

WGK 3

閃點（°F）

179.6 °F - closed cup

閃點（°C）

82 °C - closed cup

個人防護裝備

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

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分析证书(COA)

Lot/Batch Number
WXBD6911V
WXBD5836V
WXBD4051V
WXBD2291V
WXBD0462V

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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)
Synthesis of [18F] GBR 12909, a dopamine reuptake inhibitor.
Haka MS and Kilbourn MR.
Journal of Labelled Compounds & Radiopharmaceuticals, 28(7), 793-799 (1990)
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)
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)
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

The Friedel–Crafts acylation is the reaction of an arene with acyl chlorides or anhydrides using a strong Lewis acid catalyst. This reaction proceeds via electrophilic aromatic substitution to form monoacylated products.

Friedel–Crafts Acylation

The Friedel–Crafts acylation is the reaction of an arene with acyl chlorides or anhydrides using a strong Lewis acid catalyst. This reaction proceeds via electrophilic aromatic substitution to form monoacylated products.

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