4-BROMO PHTHALIC ANHYDRUS

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CAS:86-90-8
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CAS:86-90-8
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CAS:86-90-8
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4-BROMO PHTHALIC ANHYDRUS manufacturers

  • 4-BROMO PHTHALIC ANHYDRUS
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  • $5.00 / 1KG
  • 2025-09-25
  • CAS:86-90-8
  • Min. Order: 1KG
  • Purity: 99%
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4-BROMO PHTHALIC ANHYDRUS Basic information
Uses
Product Name:4-BROMO PHTHALIC ANHYDRUS
Synonyms:5-Bromo-2-Benzofuran-1,3-Dione;4-BPA;4-BROMOPHTHALIC ACID ANHYDRIDE;4-bromo-1,3-dihydro-2-benzofuran-1,3-dione;4-Bromo-isobenzofuran-1,3-dione;4-BROMO PHTHALIC ANHYDRUS;TIMTEC-BB SBB008534;5-Bromo-1,3-isobenzofurandione
CAS:86-90-8
MF:C8H3BrO3
MW:227.01
EINECS:201-707-9
Product Categories:strong recommend;Phthalic Acids, Esters and Derivatives;Furan&Benzofuran;Aryl;Organoborons;bc0001
Mol File:86-90-8.mol
4-BROMO PHTHALIC ANHYDRUS Structure
4-BROMO PHTHALIC ANHYDRUS Chemical Properties
Melting point 107 °C
Boiling point 301 °C
density 1.911
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility very soluble in Benzene
form powder to crystal
color White to Almost white
InChIInChI=1S/C8H3BrO3/c9-4-1-2-5-6(3-4)8(11)12-7(5)10/h1-3H
InChIKeyBCKVHOUUJMYIAN-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C=C(Br)C=C2)C(=O)O1
CAS DataBase Reference86-90-8(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HS Code 29173990
MSDS Information
4-BROMO PHTHALIC ANHYDRUS Usage And Synthesis
Uses4-Bromophthalic anhydride is a white or grayish-white crystalline solid at room temperature and pressure. It can be used as an intermediate in organic and biochemical synthesis, and for the derivatization of drug molecules and bioactive molecules. In addition, 4-Bromophthalic anhydride can also be used in the synthesis of dye intermediates and plant growth regulators.
Chemical Propertiesoff-white to white powder
Synthesis
Phthalic anhydride

85-44-9

4-BROMO PHTHALIC ANHYDRUS

86-90-8

To a suspension of phthalic anhydride (1) (22 g, 148.5 mmol, 1.0 eq.) in water (150 mL) was slowly added sodium hydroxide (12 g, 300.0 mmol, 2.0 eq.) and pure bromine (8.5 mL, 165.9 mmol, 1.1 eq.). The reaction mixture was stirred at 90 °C for 12 hours. Upon completion of the reaction, the mixture was cooled to 0 °C and filtered to collect a pale yellow solid. After washing the solid with cold water (50 mL), it was dissolved in sulfur dioxide (60 mL) and the mixture was heated to reflux for 5 hours. The reaction mixture was concentrated and dichloromethane (200 mL) was added to the residue and stirred at room temperature for 2 hours. After filtration, the filtrate was concentrated to give 5-bromoisobenzofuran-1,3-dione (2) (20 g, 71% yield) as a yellow solid.1H NMR (400 MHz, CDCl3) δ 8.16-8.17 (m, 1H), 8.06-8.07 (m, 1H), 7.89-7.90 (m, 1H).

References[1] Patent: CN105399712, 2016, A. Location in patent: Paragraph 0025
[2] Patent: US2010/204214, 2010, A1. Location in patent: Page/Page column 109
[3] Journal of Medicinal Chemistry, 2017, vol. 60, # 3, p. 1142 - 1150
[4] Patent: WO2018/95260, 2018, A1. Location in patent: Paragraph 058; 060; 0116
[5] Journal of Medicinal Chemistry, 1993, vol. 36, # 22, p. 3417 - 3423
Tag:4-BROMO PHTHALIC ANHYDRUS(86-90-8) Related Product Information
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