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5-bromobenzo[d]isoxazol-3-one

CAS No.
65685-50-9
Chemical Name:
5-bromobenzo[d]isoxazol-3-one
Synonyms
5-broMo-1,2-benzoxazol-3-ol;5-bromo-1,2-benzoxazol-3-one;5-Bromobenzisoxazol-3(2H)-one;5-bromobenzo[d]isoxazol-3-one;5-Bromobenzo[d]isoxazol-3(2H);5-BroMobenzo[d]isoxazol-3(2H)-one;1,2-Benzisoxazol-3(2H)-one, 5-bromo-;5-bromo-2,3-dihydro-1,2-benzoxazol-3-one
CBNumber:
CB91509086
Molecular Formula:
C7H4BrNO2
Molecular Weight:
214.02
MDL Number:
MFCD01658969
MOL File:
65685-50-9.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:52

5-bromobenzo[d]isoxazol-3-one Properties

Melting point 202-203 °C
Density 1.809±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 13.30±0.20(Predicted)
Appearance Off-white to light brown Solid

5-bromobenzo[d]isoxazol-3-one price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth Carbosynth FB141713 5-Bromobenzo[d]isoxazol-3(2H)-one 65685-50-9 50mg $82 2021-12-16 Buy
AK Scientific Z5002 5-Bromobenzo[d]isoxazol-3(2H)-one 65685-50-9 25mg $99 2021-12-16 Buy
Biosynth Carbosynth FB141713 5-Bromobenzo[d]isoxazol-3(2H)-one 65685-50-9 100mg $142 2021-12-16 Buy
AK Scientific J96303 5-Bromobenzo[d]isoxazol-3(2H)-one 65685-50-9 100mg $203 2021-12-16 Buy
Biosynth Carbosynth FB141713 5-Bromobenzo[d]isoxazol-3(2H)-one 65685-50-9 250mg $282.5 2021-12-16 Buy
Product number Packaging Price Buy
FB141713 50mg $82 Buy
Z5002 25mg $99 Buy
FB141713 100mg $142 Buy
J96303 100mg $203 Buy
FB141713 250mg $282.5 Buy

5-bromobenzo[d]isoxazol-3-one Chemical Properties,Uses,Production

Synthesis

5-Bromo-N,2-dihydroxybenzamide

5798-94-7

5-bromobenzo[d]isoxazol-3-one

65685-50-9

The general procedure for the synthesis of 5-bromobenzo[d]isoxazol-3(2H)-one from the compound (CAS:5798-94-7) was as follows: thionyl chloride (10 ml) was added slowly and dropwise to a solution of δ-bromosalicylcarbamic acid F2 (21.6 g) in tetrahydrofuran (60 ml) under stirring conditions at 10-200 °C. Stirring of the reaction mixture was continued for 2 hours by maintaining the same temperature. Subsequently, the reaction mixture was evaporated under reduced pressure to remove the solvent, the residue was dissolved in dioxane (60 ml) and the solution was cooled to 0-50 °C. To this cooled reaction mixture triethylamine (38 ml) was added and stirred at 37 °C. After that, the reaction mixture was allowed to stand at room temperature for 1 hour. The solvent was again removed by evaporation under reduced pressure and ice water (300 mL) was added to the residue. The pH of the mixture was adjusted to 2 using concentrated hydrochloric acid, at which point crystals were precipitated, and the precipitated crystals were collected by filtration and washed with water. Finally, the target compound F3 was purified by recrystallization from ethyl acetate to give the target compound F3 (17.5 g, 88% yield) as colorless needle-like crystals.

References

[1] Patent: WO2011/20615, 2011, A1. Location in patent: Page/Page column 75; 76
[2] Journal of Medicinal Chemistry, 2008, vol. 51, # 12, p. 3357 - 3359
[3] Patent: US2015/175560, 2015, A1. Location in patent: Paragraph 0468; 0470

5-bromobenzo[d]isoxazol-3-one Preparation Products And Raw materials

5-bromobenzo[d]isoxazol-3-one Suppliers

Global( 45)Suppliers
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Alchem Pharmtech,Inc.
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Career Henan Chemica Co
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Aladdin Scientific
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Amadis Chemical Company Limited
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5-bromobenzo[d]isoxazol-3-one Spectrum

65685-50-9(5-bromobenzo[d]isoxazol-3-one)Related Search:

5-bromobenzo[d]isoxazol-3-one 5-broMo-1,2-benzoxazol-3-ol 5-BroMobenzo[d]isoxazol-3(2H)-one 5-Bromobenzo[d]isoxazol-3(2H) 5-bromo-1,2-benzoxazol-3-one 1,2-Benzisoxazol-3(2H)-one, 5-bromo- 5-Bromobenzisoxazol-3(2H)-one 5-bromo-2,3-dihydro-1,2-benzoxazol-3-one 65685-50-9