3-Hydroxy-2-methylbenzoic acid
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
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)
MSDS
- Language:English Provider:ALFA
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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