ChemicalBook--->CAS DataBase List--->33763-20-1

33763-20-1

33763-20-1 Structure

33763-20-1 Structure
IdentificationMore
[Name]

4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID
[CAS]

33763-20-1
[Synonyms]

4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID
4-METHYL-2-PHENYL-THIAZOLE-5-CARBOXYLIC ACID
AKOS BBS-00004452
IFLAB-BB F1912-0027
4-Methyl-2-phenyl-5-thiazolecarboxylicacid
4-Methyl-2-phenyl-1,3-thiazole-5-carboxylic acid ,97%
[Molecular Formula]

C11H9NO2S
[MDL Number]

MFCD00141955
[Molecular Weight]

219.26
[MOL File]

33763-20-1.mol
Chemical PropertiesBack Directory
[Melting point ]

210-212°C
[Boiling point ]

424.0±37.0 °C(Predicted)
[density ]

1.319±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

1.20±0.37(Predicted)
[Appearance]

White to off-white Solid
[Detection Methods]

HPLC
[CAS DataBase Reference]

33763-20-1(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S22:Do not breathe dust .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[HazardClass ]

IRRITANT
[HS Code ]

29349990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sodium hydroxide-->Ethyl 2-chloroacetoacetate-->THIOBENZAMIDE-->4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBONYL CHLORIDE-->ETHYL 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLATE-->Methanol
[Preparation Products]

4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBONYL CHLORIDE-->4-ethyl-2-phenyl-5-Thiazolecarboxylic acid
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Uses]

4-Methyl-2-phenyl-1,3-thiazole-5-carboxylic Acid is a useful reagent in Pd-catalyzed decarboxylative C-H cross-coupling of oxazoles and thiazoles.
[Synthesis]

ETHYL 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLATE

53715-64-3

4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID

33763-20-1

General method: 2N aqueous sodium hydroxide solution was slowly added to a methanol solution containing ethyl 4-methyl-2-phenyl-1,3-thiazole-5-carboxylate (1 eq.) at room temperature. The reaction mixture was stirred continuously for 4 hours at room temperature. After completion of the reaction, the methanol solvent was removed by rotary evaporator. Subsequently, the pH of the reaction mixture was adjusted to 5-6 with 1N hydrochloric acid solution.The precipitated white solid was collected by filtration and processed by drying to finally give 4-methyl-2-phenylthiazole-5-carboxylic acid (1a-i).

[References]

[1] Journal of Medicinal Chemistry, 2007, vol. 50, # 4, p. 685 - 695
[2] European Journal of Medicinal Chemistry, 2017, vol. 137, p. 96 - 107
[3] Justus Liebigs Annalen der Chemie, 1974, p. 1195 - 1205
[4] Heterocycles, 2014, vol. 89, # 2, p. 453 - 464
[5] Molecules, 2014, vol. 19, # 7, p. 9240 - 9256
Spectrum DetailBack Directory
[Spectrum Detail]

4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLIC ACID(33763-20-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

4-methyl-2-phenyl-1,3-thiazole-5-carboxylic acid(33763-20-1)
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