ChemicalBook--->CAS DataBase List--->81015-49-8

81015-49-8

81015-49-8 Structure

81015-49-8 Structure
IdentificationBack Directory
[Name]

4-(2-THIAZOLYL)PHENOL
[CAS]

81015-49-8
[Synonyms]

4-(2-Thiazolyl)
4-(2-THIAZOLYL)PHENOL
4-(2-Thiazolyl)phenol8
Phenol, 4-(2-thiazolyl)-
4-(2-Thiazolyl)phenol95%
4-(2-THIAZOLYL)PHENOL 95%
2-(4-chlorophenyl)thiazole
4-(1,3-Thiazol-2-yl)phenol
4-(3H-1,3-thiazol-2-ylidene)cyclohexa-2,5-dien-1-one
[Molecular Formula]

C9H7NOS
[MDL Number]

MFCD07368615
[MOL File]

81015-49-8.mol
[Molecular Weight]

177.22
Chemical PropertiesBack Directory
[Melting point ]

162-165℃
[storage temp. ]

Store at room temperature
[Appearance]

Light yellow to yellow Solid
[CAS DataBase Reference]

81015-49-8
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280h-P305+P351+P338
[HS Code ]

2934100090
Spectrum DetailBack Directory
[Spectrum Detail]

4-(2-THIAZOLYL)PHENOL(81015-49-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-(4-methoxyphenyl)-1,3-thiazole

27088-84-2

4-(2-THIAZOLYL)PHENOL

81015-49-8

Step 2: Synthesis of 4-thiazol-2-yl-phenol; Boron tribromide (2.00 ml, 15.7 mmol) was added slowly and dropwise to a solution of dichloromethane (25 ml) of the product obtained in step 1 (1.0 g, 5.23 mmol) at -78 °C, keeping the temperature at -78 °C and stirring the reaction for 1 hour. Subsequently, the reaction mixture was warmed to room temperature and stirring was continued for 16 hours. After completion of the reaction, the reaction was quenched by slowly pouring the mixture into ice water. The solid product was collected by filtration and washed with ether to give the final target product 4-thiazol-2-yl-phenol (0.84 g, 84% yield); 1H NMR (400 MHz, CDCl3) δ 7.85 (d, J = 3.2Hz, 1H), 7.79 (d, J = 8.8Hz, 2H), 7.67 (d, J = 3.2Hz, 1H), 7.67 (d, J = 3.2Hz, 1H), 7.67 (d, J = 3.2Hz, 1H), and 6.88 (d, J = 8.8 Hz, 2H); MS (ESI-) m/z 176 ([M-H]-, 100).

[References]

[1] European Journal of Medicinal Chemistry, 2010, vol. 45, # 6, p. 2299 - 2306
[2] Patent: US2007/66820, 2007, A1. Location in patent: Page/Page column 78
[3] Patent: US2008/33024, 2008, A1. Location in patent: Page/Page column 7; 16
[4] Journal of Medicinal Chemistry, 1986, vol. 29, # 6, p. 1065 - 1080
[5] Journal of the American Chemical Society, 1930, vol. 52, p. 1585
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