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3-Hydroxy-2-methylbenzoic acid

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3-Hydroxy-2-methylbenzoic acid Basic information

Product Name:
3-Hydroxy-2-methylbenzoic acid
Synonyms:
  • 2-Methyl-3-hydroxybenzoicacid
  • HMBA
  • 3-HYDROXY-O-TOLUIC ACID
  • 3-HYDROXY-2-TOLUIC ACID
  • 3-HYDROXY-2-METHYLBENZOIC ACID
  • Hydroxytoluicacid,98%
  • 3,2-Cresotic Acid
  • NSC 73133
CAS:
603-80-5
MF:
C8H8O3
MW:
152.15
EINECS:
629-955-7
Product Categories:
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Pesticide Intermediate
  • Organic acids
  • Aromatics Compounds
  • Aromatics
  • Nelfinavir Mesylate
  • Acids and Derivatives
  • Alcohols and Derivatives
  • bc0001
Mol File:
603-80-5.mol
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3-Hydroxy-2-methylbenzoic acid Chemical Properties

Melting point:
143-148°C
Boiling point:
336.6±30.0 °C(Predicted)
Density 
1.304±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
3.83±0.10(Predicted)
color 
Light Yellow
BRN 
2613791
InChI
InChI=1S/C8H8O3/c1-5-6(8(10)11)3-2-4-7(5)9/h2-4,9H,1H3,(H,10,11)
InChIKey
RIERSGULWXEJKL-UHFFFAOYSA-N
SMILES
C(O)(=O)C1=CC=CC(O)=C1C
CAS DataBase Reference
603-80-5(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36
HazardClass 
IRRITANT
HS Code 
29182900

MSDS

  • Language:English Provider:ALFA
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3-Hydroxy-2-methylbenzoic acid Usage And Synthesis

Chemical Properties

Light Yellow Crystalline Solid

Uses

3-Hydroxy-2-methylbenzoic Acid (cas# 603-80-5) is a compound useful in organic synthesis.

Synthesis

52130-17-3

603-80-5

General procedure for the synthesis of 2-methyl-3-hydroxybenzoic acid from 3-amino-2-methylbenzoic acid: to 5 mL of water containing 0.65 mL of concentrated sulfuric acid, a cold (0°C) suspension of 0.54 g (3.3 mmol) of 2-methyl-3-aminobenzoic acid was added, followed by 0.25 g (3.6 mmol) of solid sodium nitrite. After about 15 minutes of reaction, the mixture was poured into 20 mL of warm water containing 4 mL of concentrated sulfuric acid. The reaction mixture was slowly heated to 90°C and gas was observed to escape. When gas release ceased, the solution was cooled to room temperature and extracted with ethyl acetate. The organic layers were combined, washed with 0.5 N hydrochloric acid, dried and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: 5% dichloromethane solution in methanol) to give 350 mg of white solid (melting point: 137-138°C) in 69% yield.1H NMR (CDCl3) data: δ 8.18 (br.s, 1H), 7.42 (d, J = 7.7 Hz, 1H), 7.13 (t, J = 7.9 Hz, 1H) , 6.93 (d, J = 7.9 Hz, 1H), 2.46 (s, 3H). Elemental analysis (C8H8O3) results: calculated values: C, 63.15; H, 5.29; measured values: C, 63.32; H, 5.36.

References

[1] Patent: US6335/459, 2002, B1. Location in patent: Page column 29
[2] Patent: US6335459, 2002, B1. Location in patent: Page column 29
[3] Tetrahedron Letters, 2000, vol. 41, # 11, p. 1741 - 1745
[4] Patent: US5952343, 1999, A
[5] Patent: US5484926, 1996, A

3-Hydroxy-2-methylbenzoic acid Preparation Products And Raw materials

Raw materials

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