ChemicalBook--->CAS DataBase List--->1984-58-3

1984-58-3

1984-58-3 Structure

1984-58-3 Structure
IdentificationMore
[Name]

2,5-DICHLOROANISOLE
[CAS]

1984-58-3
[Synonyms]

1,4-DICHLORO-2-METHOXYBENZENE
2,5-DICHLOROANISOLE
2,5-DICHLOROMETHOXYBENZENE
1,4-dichloro-2-methoxy-benzen
2,5-DICHLOROANISOLE 99%
Banair
[EINECS(EC#)]

217-852-6
[Molecular Formula]

C7H6Cl2O
[MDL Number]

MFCD00061123
[Molecular Weight]

177.03
[MOL File]

1984-58-3.mol
Chemical PropertiesBack Directory
[Appearance]

clear colorless to very slightly yellow liquid
[Melting point ]

24°C
[Boiling point ]

128-132°C 3,5mm
[density ]

1.33
[refractive index ]

1.5615-1.5635
[Fp ]

21°C
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

Liquid
[color ]

Clear colorless to very slightly yellow
[BRN ]

2327401
[CAS DataBase Reference]

1984-58-3(CAS DataBase Reference)
[EPA Substance Registry System]

2,5-Dichloroanisole (1984-58-3)
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R20/22:Harmful by inhalation and if swallowed .
[Safety Statements ]

S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
[RIDADR ]

1993
[Hazard Note ]

Irritant
[TSCA ]

Yes
[HS Code ]

29093090
Hazard InformationBack Directory
[Chemical Properties]

clear colorless to very slightly yellow liquid
[Uses]

1,4-Dichloro-2-methoxybenzene is a useful reagent for organic synthesis.
[Synthesis]

Methanol

67-56-1

1,2,4-Trichlorobenzene

120-82-1

2,5-Dichlorophenol

583-78-8

3,4-Dichlorophenol

95-77-2

2,4-DICHLOROANISOLE

553-82-2

2,5-DICHLOROANISOLE

1984-58-3

2,4-Dichlorophenol

120-83-2

3,4-DICHLOROANISOLE

36404-30-5

1,2,4-Trichlorobenzene (TCB), 50 wt% aqueous NaOH and methanol were added to a pressure reactor at a molar ratio of 1.0:2.4:10. The reactor was sealed and heated to 190°C under stirring conditions and maintained at this temperature for 90 minutes. Continuous stirring was maintained during the reaction. Upon completion of the reaction, the reactor was cooled to room temperature using an ice water bath. The reaction mixture was transferred to a separatory funnel and acidified with 10% H2SO4 to a pH below 1.5. Subsequently, dichloromethane was extracted three times with an aqueous layer. The final yield of 2,5-dichlorophenol was 64.6%. The ratio of regioselectivity (2,5-dichlorophenol to 2,5-dichloroanisole/2,4-dichlorophenol to 2,4-dichloroanisole/3,4-dichlorophenol to 3,4-dichloroanisole) was 71.9:15.5:12.6 as analyzed by gas chromatography (GC).

[References]

[1] Patent: WO2015/49160, 2015, A1. Location in patent: Page/Page column 11
[2] Patent: WO2015/49360, 2015, A1. Location in patent: Page/Page column 14
Spectrum DetailBack Directory
[Spectrum Detail]

2,5-DICHLOROANISOLE(1984-58-3)MS
2,5-DICHLOROANISOLE(1984-58-3)1HNMR
2,5-DICHLOROANISOLE(1984-58-3)13CNMR
2,5-DICHLOROANISOLE(1984-58-3)IR1
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2,5-Dichloroanisole, 99%(1984-58-3)
[Alfa Aesar]

2,5-Dichloroanisole, 98%(1984-58-3)
[TCI AMERICA]

2,5-Dichloroanisole,>98.0%(GC)(1984-58-3)
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