ChemicalBook > CAS DataBase List > 4'-Fluoropropiophenone

4'-Fluoropropiophenone

Product Name
4'-Fluoropropiophenone
CAS No.
456-03-1
Chemical Name
4'-Fluoropropiophenone
Synonyms
p-fluorophenone;Fluorophenylacetone;P-FLUOROPROPIOPHENONE;4-FLUOROPROPIOPHENONE;LABOTEST-BB LT01148316;4'-fluoropropiophenone;para-Fluoropropiophenone;4-Fluoropropiophenone99%;Propiophenone, 4'-fluoro-;4-Fluoropropiophenone 99%
CBNumber
CB1700848
Molecular Formula
C9H9FO
Formula Weight
152.17
MOL File
456-03-1.mol
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4'-Fluoropropiophenone Property

Boiling point:
100-102 °C (22 mmHg)
Density 
1.096 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.5059(lit.)
Flash point:
170 °F
storage temp. 
Inert atmosphere,Room Temperature
form 
clear liquid
color 
Colorless to Light orange to Yellow
Specific Gravity
1.096
BRN 
1210310
InChI
InChI=1S/C9H9FO/c1-2-9(11)7-3-5-8(10)6-4-7/h3-6H,2H2,1H3
InChIKey
QIJNVLLXIIPXQT-UHFFFAOYSA-N
SMILES
C(C1=CC=C(F)C=C1)(=O)CC
CAS DataBase Reference
456-03-1(CAS DataBase Reference)
NIST Chemistry Reference
1-Propanone, 1-(4-fluorophenyl)-(456-03-1)
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Safety

Hazard Codes 
Xn,Xi
Risk Statements 
22-37/38-41-36/37/38
Safety Statements 
26-39-37/39
RIDADR 
2735
WGK Germany 
2
Hazard Note 
Irritant
HS Code 
29147000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H227Combustible liquid

H302Harmful if swallowed

H315Causes skin irritation

H318Causes serious eye damage

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P403+P235Store in a well-ventilated place. Keep cool.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
128414
Product name
4′-Fluoropropiophenone
Purity
98%
Packaging
5g
Price
$48.3
Updated
2023/01/07
TCI Chemical
Product number
F0522
Product name
4'-Fluoropropiophenone
Purity
>97.0%(GC)
Packaging
5g
Price
$17
Updated
2025/07/31
TCI Chemical
Product number
F0522
Product name
4'-Fluoropropiophenone
Purity
>97.0%(GC)
Packaging
25g
Price
$26
Updated
2025/07/31
TRC
Product number
F598745
Product name
4''-Fluoropropiophenone
Packaging
500mg
Price
$45
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0023878
Product name
4'-FLUOROPROPIOPHENONE
Purity
95.00%
Packaging
100G
Price
$2397.32
Updated
2021/12/16
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4'-Fluoropropiophenone Chemical Properties,Usage,Production

Chemical Properties

clear yellow liquid after melting

Uses

4′-Fluoropropiophenone was used in the preparation of 2-(4-fluorophenyl)-3-methylquinoxaline.

Synthesis

5724-03-8

456-03-1

General procedure for the synthesis of 4'-fluoropropiophenone from 1-(4-fluorophenyl)prop-2-en-1-ol: Under nitrogen protection, the ruthenium complex [RuCl2(6-C6H6)(PTA-Me)] (3a) (0.02-0.1 mmol; 0.5-2.5 mol%) and K2CO3 (0.05-0.25 mmol) were added to a solution of 1-(4-fluorophenyl)prop-2-en-1-ol (4a-o, 4 mmol) in tetrahydrofuran (4mL). -fluorophenyl)prop-2-en-1-ol (4a-o, 4 mmol) in a solution of tetrahydrofuran (4 mL). The reaction mixture was placed in a sealed tube and stirred at 75°C for the indicated time (see Table 4 and Scheme 3). The progress of the reaction was monitored by sampling and diluting 10 μL of the sample with dichloromethane (3 mL) every ~1 hr followed by GC analysis. Upon completion of the reaction, the mixture was cooled to room temperature, at which point the ruthenium complex 3a partially precipitated. The solids were removed by filtration and the reaction products were subsequently separated by solvent evaporation. The residue was purified using silica gel column chromatography with EtOAc-hexane (1:10) mixed solvent as eluent. The structure of the resulting carbonyl compounds 5a-o was confirmed by GC/MS analysis of their fragmentation patterns, NMR spectroscopy, and comparison of retention times of commercially pure samples (Sigma-Aldrich or Acros Organics).

References

[1] Tetrahedron, 2008, vol. 64, # 51, p. 11745 - 11750
[2] Journal of Molecular Catalysis A: Chemical, 2013, vol. 366, p. 390 - 399
[3] European Journal of Organic Chemistry, 2017, vol. 2017, # 26, p. 3886 - 3895
[4] Green Chemistry, 2010, vol. 12, # 9, p. 1628 - 1633
[5] Organometallics, 2012, vol. 31, # 23, p. 8301 - 8311

4'-Fluoropropiophenone Preparation Products And Raw materials

Raw materials

Preparation Products

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4'-Fluoropropiophenone Suppliers

Ricci Chimica
Tel
--
Fax
--
Email
sales@riccichimica.com
Country
Italy
ProdList
2146
Advantage
46
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View Lastest Price from 4'-Fluoropropiophenone manufacturers

RongNa Biotechnology Co.,Ltd
Product
4'-Fluoropropiophenone 456-03-1
Price
US $10.00/ASSAYS
Min. Order
1ASSAYS
Purity
99%
Supply Ability
10 ton
Release date
2025-05-04
Hebei Zhuanglai Chemical Trading Co Ltd
Product
4'-Fluoropropiophenone 456-03-1
Price
US $99.00-45.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-12-19
Shandong Hanjiang Chemical Co., Ltd
Product
4'-Fluoropropiophenone 456-03-1
Price
US $0.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10T
Release date
2024-01-19

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  • 456-03-1