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ChemicalBook--->CAS DataBase List--->3621-82-7

3621-82-7

3621-82-7 Structure

3621-82-7 Structure
IdentificationMore
[Name]

2,6-Dichlorobenzoxazole
[CAS]

3621-82-7
[Synonyms]

2,6-DICHLOROBENZOXAZOLE
2,6-DICHLOROBENZOXAZOLE 99+%
Benzoxazole, 2,6-dichloro-
[EINECS(EC#)]

222-818-9
[Molecular Formula]

C7H3Cl2NO
[MDL Number]

MFCD07368635
[Molecular Weight]

188.01
[MOL File]

3621-82-7.mol
Chemical PropertiesBack Directory
[Melting point ]

49-51°C
[Boiling point ]

110°C/13mmHg(lit.)
[density ]

1.522±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

fused solid
[pka]

-0.96±0.30(Predicted)
[color ]

White
[InChI]

InChI=1S/C7H3Cl2NO/c8-4-1-2-5-6(3-4)11-7(9)10-5/h1-3H
[InChIKey]

LVVQTPZQNHQLOM-UHFFFAOYSA-N
[SMILES]

O1C2=CC(Cl)=CC=C2N=C1Cl
[CAS DataBase Reference]

3621-82-7(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HS Code ]

2934999090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrochloric acid-->Chlorine-->2-Benzoxazolinone-->6-CHLORO-1,3-BENZOXAZOL-2(3H)-ONE-->6-Chloro-2-benzoxazolethiol-->2-Amino-5-chlorophenol-->2-Aminophenol-->Triphosgene-->1,2-Dichlorobenzene-->Toluene
[Preparation Products]

FENOXAPROP-ETHYL
Hazard InformationBack Directory
[Uses]

2,6-Dichlorobenzoxazole is used in the synthesis of 2-(3-(2,6-dichloro-4-(3,3-dichloroallyloxy)phenoxy)propoxy)-5-(trifluoromethyl)benzo[d]oxazole, an insecticide against Spodoptera exigua.
[Synthesis]

6-Chloro-2-benzoxazolethiol

22876-20-6

2,6-Dichlorobenzoxazole

3621-82-7

General procedure for the synthesis of 2,6-dichlorobenzoxazole from 6-chlorobenzo[d]oxazole-2(3H)-thione: In a 500-mL four-neck reaction flask, 50 g (0.27 mol) of 6-chlorobenzo[d]oxazole-2(3H)-thione, 300 mL of toluene, and 40 g (0.135 mol) of tris(trichloromethyl)carbonate were added. The reaction mixture was slowly warmed to 50°C and the temperature was continued at a rate of 0.5°C/min, holding the temperature for 10 minutes after each 10°C increase. When the temperature reached 105°C, the reaction was maintained for 1 hour. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure (the initial vacuum was maintained at -0.07 MPa, and when the temperature was raised to 100°C-110°C, the vacuum was increased to -0.095 MPa to completely evaporate the solvent). After evaporation, the residue was removed while hot and cooled and crystallized to give 50.82 g of 2,6-dichlorobenzoxazole with a product purity of 98.1% and a molar yield of 98.4%.

[References]

[1] Patent: CN102432559, 2016, B. Location in patent: Paragraph 0020; 0037; 0038
[2] Patent: WO2018/37223, 2018, A1. Location in patent: Page/Page column 197; 198
[3] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 7, p. 1975 - 1980
[4] Journal of Organic Chemistry, 2009, vol. 74, # 8, p. 3229 - 3231
[5] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 9, p. 3044 - 3049
Spectrum DetailBack Directory
[Spectrum Detail]

2,6-Dichlorobenzoxazole(3621-82-7)1HNMR
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