2,2',4'-Trichloroacetophenone
- Product Name
- 2,2',4'-Trichloroacetophenone
- CAS No.
- 4252-78-2
- Chemical Name
- 2,2',4'-Trichloroacetophenone
- Synonyms
- 2-CHLORO-1-(2,4-DICHLOROPHENYL)ETHANONE;TRICHLOROACETOPHENONE;2,2′,4′-Trichloracetophenon;Ethanone, 2-chloro-1-(2,4-dichlorophenyl)-;alpha-2,4-Tric;2,2',4'-TrichL;2,2',4-Trichloro;TRICHLOROACETOPHENON;Econazole Impurity 11;LABOTEST-BB LT00233191
- CBNumber
- CB9689842
- Molecular Formula
- C8H5Cl3O
- Formula Weight
- 223.48
- MOL File
- 4252-78-2.mol
2,2',4'-Trichloroacetophenone Property
- Melting point:
- 47-54 °C(lit.)
- Boiling point:
- 130-135 °C4 mm Hg(lit.)
- Density
- 1,312 g/cm3
- refractive index
- 1.5510 (estimate)
- Flash point:
- >230 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- 60 mg/L (20°C)
- form
- Solid
- color
- beige to yellow
- PH
- 4.96 at 25.1℃ and 10g/L
- Water Solubility
- 60 mg/L (20 ºC)
- Sensitive
- Lachrymatory
- BRN
- 957098
- CAS DataBase Reference
- 4252-78-2(CAS DataBase Reference)
- EPA Substance Registry System
- Ethanone, 2-chloro-1-(2,4-dichlorophenyl)- (4252-78-2)
Safety
- Hazard Codes
- Xi,C,N,T
- Risk Statements
- 37/38-41-43-51/53-34-23/24/25
- Safety Statements
- 26-36/37/39-61-45-37/39
- RIDADR
- 1759
- WGK Germany
- 3
- Hazard Note
- Corrosive/Lachrymatory
- HazardClass
- 8
- PackingGroup
- III
- HS Code
- 29147090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H315Causes skin irritation
H317May cause an allergic skin reaction
H318Causes serious eye damage
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
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.
N-Bromosuccinimide Price
- Product number
- 159255
- Product name
- 2,2′,4′-Trichloroacetophenone
- Purity
- 97%
- Packaging
- 25g
- Price
- $61.7
- Updated
- 2025/07/31
- Product number
- T1405
- Product name
- 2,2',4'-Trichloroacetophenone
- Purity
- >98.0%(GC)
- Packaging
- 25g
- Price
- $40
- Updated
- 2025/07/31
- Product number
- T1405
- Product name
- 2,2',4'-Trichloroacetophenone
- Purity
- >98.0%(GC)
- Packaging
- 250g
- Price
- $223
- Updated
- 2025/07/31
- Product number
- T774315
- Product name
- α,2,4-Trichloroacetophenone
- Packaging
- 100g
- Price
- $250
- Updated
- 2021/12/16
- Product number
- T774315
- Product name
- α,2,4-Trichloroacetophenone
- Packaging
- 50g
- Price
- $150
- Updated
- 2021/12/16
2,2',4'-Trichloroacetophenone Chemical Properties,Usage,Production
Chemical Properties
yellow crystalline powde
Uses
α,2,4-Trichloroacetophenone is a reagent used in the synthesis of isoconazole, a potent antifungal agent.
General Description
Off-white crystalline solid.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
2,2',4'-Trichloroacetophenone is incompatible with strong oxidizers and strong bases. .
Fire Hazard
2,2',4'-Trichloroacetophenone is probably combustible.
Synthesis
79-04-9
541-73-1
4252-78-2
To a three-necked flask equipped with a stirrer was added 1,3-dichlorobenzene (147 g), chloroacetyl chloride (113 g) and methylene chloride (750 mL) at room temperature. Under stirring, anhydrous aluminum trichloride (147 g) was added in batches. After the addition was complete, the reaction mixture was heated to reflux and maintained for 3 hours to ensure complete reaction. Upon completion of the reaction, the mixture was quenched by carefully pouring it into ice water. Subsequently, the organic and aqueous phases were separated. The organic phase was washed sequentially with deionized water (500 mL x 2) and saturated sodium bicarbonate solution (500 mL x 2) to remove acidic impurities. The washed organic phase was dried with anhydrous sodium sulfate and filtered to remove the desiccant. The filtrate was concentrated by rotary evaporation and petroleum ether (1200 mL) was added to the residue. The mixture was cooled to room temperature and placed in a refrigerator overnight to promote crystallization. The following day, the crystallized product was collected by filtration and washed with a small amount of cold petroleum ether. Ultimately, the product was dried under vacuum to give 2,2',4'-trichloroacetophenone (193 g, 86% yield) in the form of an off-white solid.
References
[1] Journal of Chemical Sciences, 2015, vol. 127, # 12, p. 2251 - 2260
[2] Patent: CN105566309, 2016, A. Location in patent: Paragraph 0003; 0007
[3] Chemische Berichte, 1907, vol. 40, p. 1703
[4] Tetrahedron Asymmetry, 2003, vol. 14, # 24, p. 3861 - 3866
[5] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 20, p. 5368 - 5371
2,2',4'-Trichloroacetophenone Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 2,2',4'-Trichloroacetophenone manufacturers
- Product
- 2,2',4'-Trichloroacetophenone 4252-78-2
- Price
- US $0.00-0.00/kg
- Min. Order
- 1kg
- Purity
- 99%+
- Supply Ability
- 100000kgs per month
- Release date
- 2024-04-07
- Product
- 2,2',4'-Trichloroacetophenone 4252-78-2
- Price
- US $50.00/kg
- Min. Order
- 1kg
- Purity
- 99
- Supply Ability
- 5000
- Release date
- 2024-12-06
- Product
- 2,2',4'-Trichloroacetophenone 4252-78-2
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 1ton
- Release date
- 2022-10-10