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2,4-Dihydroxybenzamide

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Products Intro: Product Name:2,4-Dihydroxybenzamide
CAS:3147-45-3
Purity:98% Package:25kg;5KG;1KG
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Products Intro: Product Name:2,4-Dihydroxybenzamide
CAS:3147-45-3
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CAS:3147-45-3
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Products Intro: Product Name:2,4-Dihydroxybenzamide
CAS:3147-45-3
Purity:98% Package:1KG;1USD
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Products Intro: Product Name:2,4-Dihydroxybenzamide
CAS:3147-45-3
Purity:97% Package:10G 100G 1KG 25KG

2,4-Dihydroxybenzamide manufacturers

  • 2,4-Dihydroxybenzamide
  • 2,4-Dihydroxybenzamide pictures
  • $0.00 / 1kg
  • 2023-03-13
  • CAS:3147-45-3
  • Min. Order: 1kg
  • Purity: 98%Min
  • Supply Ability: 1000kg
2,4-Dihydroxybenzamide Basic information
Product Name:2,4-Dihydroxybenzamide
Synonyms:B-RESORCYL AMIDE;2,4-DIHYDROXY BENZOYLAMINE;2,4-DIHYDROXYBENZAMIDE;4-HYDROXY SALICYLAMIDE;2,4-Dihydroxybenzamide(P-Hydroxysalicylamide);2,4-dihydroxy-benzamid;p-hydroxysaliamide;P-Hydroxysalicylamide
CAS:3147-45-3
MF:C7H7NO3
MW:153.14
EINECS:221-567-2
Product Categories:Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
Mol File:3147-45-3.mol
2,4-Dihydroxybenzamide Structure
2,4-Dihydroxybenzamide Chemical Properties
Melting point 228 °C
Boiling point 455.8±15.0 °C(Predicted)
density 1.458±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka8.15±0.10(Predicted)
color White to Light red to Green
InChIInChI=1S/C7H7NO3/c8-7(11)5-2-1-4(9)3-6(5)10/h1-3,9-10H,(H2,8,11)
InChIKeyIIUJCQYKTGNRHH-UHFFFAOYSA-N
SMILESC(N)(=O)C1=CC=C(O)C=C1O
CAS DataBase Reference3147-45-3(CAS DataBase Reference)
EPA Substance Registry SystemBenzamide, 2,4-dihydroxy- (3147-45-3)
Safety Information
HS Code 2924.29.7790
MSDS Information
2,4-Dihydroxybenzamide Usage And Synthesis
Uses2,4-Dihydroxybenzamide is a specific inhibitor of glutathione reductase.
Synthesis General procedure for preparation of 2,4-dihydroxybenzamide. It was prepared by the addition of 1.69 g (0.10 mol) methyl 2,4-dihydroxybenzoate in 10 mL of ammonia (pro analysis, 25% in water). The reaction mixture was stirred for 24 hours at room temperature. The excess ammonia and methanol formed during the reaction were removed under reduced pressure. Upon addition of 10 mL of water, the product was extracted by ether. Ether extracts were collected and washed with water, and after separation, the ether layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure to give 2,4-dihydroxy benzamide. Crude products were purified by column chromatography using ethyl acetate as a mobile phase[1].
References[1] Milena Jadrijevi?-Mladar Takac, Drazen Viki? Topi?. “FT-IR and NMR spectroscopic studies of salicylic acid derivatives. II. Comparison of 2-hydroxy- and 2,4- and 2,5-dihydroxy derivatives.” Acta Pharmaceutica 54 3 (2004): 177–91.
Tag:2,4-Dihydroxybenzamide(3147-45-3) Related Product Information
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