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119946

4-Fluorobenzoyl chloride

98%

Synonym(s):

4-Fluorobenzoic acid chloride, p-Fluorobenzoyl chloride

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About This Item

Linear Formula:
FC6H4COCl
CAS Number:
403-43-0
Molecular Weight:
158.56
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847304
EC Number:
206-961-4
Beilstein/REAXYS Number:
386215
MDL number:
MFCD00000684
Assay:
98%
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Quality Level

200

assay

98%

refractive index

n20/D 1.532 (lit.)

bp

82 °C/20 mmHg (lit.)

mp

10-12 °C (lit.)

density

1.342 g/mL at 25 °C (lit.)

functional group

acyl chloride, fluoro

SMILES string

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

General description

4-Fluorobenzoyl chloride undergoes Friedel-Crafts acylation reaction with 2,6-dimethylnaphthalene to give 1,5-bis(4-fluorobenzoyl)-2,6-dimethylnaphthalene.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

179.6 °F - closed cup

flash_point_c

82 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
WXBD6911V
WXBD5836V
WXBD4051V
WXBD2291V
WXBD0462V

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Articles

傅-克酰基化反应

傅-克酰基化反应是一种芳烃与酰氯或酸酐使用强路易斯酸催化剂的反应。该反应通过亲电芳族取代进行，形成单酰化产物。

Friedel–Crafts Acylation

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

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He L, et al.
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Haka MS and Kilbourn MR.
Journal of Labelled Compounds & Radiopharmaceuticals, 28(7), 793-799 (1990)
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Global Trade Item Number

SKUGTIN
119946-100G04061838345325
119946-25G04061838712370
119946-5G04061838712387