ChemicalBook--->CAS DataBase List--->1184181-48-3

1184181-48-3

1184181-48-3 Structure

1184181-48-3 Structure
IdentificationBack Directory
[Name]

2,4-Dihydroxy-5-isopropylbenzoic acid
[CAS]

1184181-48-3
[Synonyms]

2,4-Dihydroxy-5-isopropylbenzoic acid
2,4-DIHYDROXY-5-(PROPAN-2-YL)BENZOIC ACID
Benzoic acid, 2,4-dihydroxy-5-(1-methylethyl)-
2,4-Dihydroxy-5-isopropylbenzoic acid ISO 9001:2015 REACH
[Molecular Formula]

C10H12O4
[MDL Number]

MFCD16996083
[MOL File]

1184181-48-3.mol
[Molecular Weight]

196.2
Chemical PropertiesBack Directory
[Boiling point ]

395.2±27.0 °C(Predicted)
[density ]

1.317±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

3.48±0.10(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C10H12O4/c1-5(2)6-3-7(10(13)14)9(12)4-8(6)11/h3-5,11-12H,1-2H3,(H,13,14)
[InChIKey]

JAMMFVLHQOLNOP-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC(C(C)C)=C(O)C=C1O
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P305+P351+P338-P337+P313-P261-P271-P304+P340-P312-P403+P233-P405-P501
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-Dihydroxy-5-isopropylbenzoic acid(1184181-48-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 2,4-dihydroxy-5-isopropylbenzoate

943519-37-7

2,4-Dihydroxy-5-isopropylbenzoic acid

1184181-48-3

General procedure for the synthesis of 2,4-dihydroxy-5-isopropylbenzoic acid from methyl 2,4-dihydroxy-5-isopropylbenzoate: the reaction was carried out by stirring the methyl 2,4-dihydroxy-5-isopropylbenzoate (0.24 g, 0.97 mmol) with lithium hydroxide (1 g) in a solvent mixture of methanol (10 mL) and water (10 mL) for 12 h at 50 °C, the reaction was was carried out under argon protection and equipped with a reflux condenser. Upon completion of the reaction, the reaction mixture was neutralized to pH 6 with 6N hydrochloric acid and subsequently extracted three times with ethyl acetate. The organic layers were combined, dried with anhydrous sodium sulfate, concentrated under reduced pressure and finally purified by medium pressure liquid chromatography (MPLC) to afford 2,4-dihydroxy-5-isopropylbenzoic acid in 100% yield. The thin layer chromatography (TLC) Rf value was 0.23 (ethyl acetate:hexane = 3:7).1H NMR (400 MHz, CD3OD) δ 7.68 (s, 1H), 6.35 (s, 1H), 3.25-3.22 (m, 1H), 1.27 (d, J = 4.0 Hz, 6H).13C NMR (100 MHz, CD3OD) δ 173.8, 163.3, 163.1, 129.2, 128.7, 105.4, 103.1, 27.7, 23.2.

[References]

[1] European Journal of Medicinal Chemistry, 2016, vol. 124, p. 1069 - 1080
[2] Patent: KR101789269, 2017, B1. Location in patent: Paragraph 0046; 0048; 0057; 0058
[3] European Journal of Medicinal Chemistry, 2018, vol. 143, p. 390 - 401
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