4-(2-THIAZOLYL)PHENOL
- Product Name
- 4-(2-THIAZOLYL)PHENOL
- CAS No.
- 81015-49-8
- Chemical Name
- 4-(2-THIAZOLYL)PHENOL
- 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%;4-(1,3-Thiazol-2-yl)phenol;2-(4-chlorophenyl)thiazole;4-(3H-1,3-thiazol-2-ylidene)cyclohexa-2,5-dien-1-one
- CBNumber
- CB0466905
- Molecular Formula
- C9H7NOS
- Formula Weight
- 177.22
- MOL File
- 81015-49-8.mol
4-(2-THIAZOLYL)PHENOL Property
- Melting point:
- 162-165℃
- storage temp.
- Store at room temperature
- Appearance
- Light yellow to yellow Solid
- CAS DataBase Reference
- 81015-49-8
Safety
- HS Code
- 2934100090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- T430125
- Product name
- 4-(2-Thiazolyl)phenol
- Packaging
- 25mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- W8566
- Product name
- 4-(2-Thiazolyl)phenol
- Packaging
- 100mg
- Price
- $95
- Updated
- 2021/12/16
- Product number
- OR913227
- Product name
- 4-(2-Thiazolyl)phenol
- Purity
- 95%
- Packaging
- 1g
- Price
- $115
- Updated
- 2021/12/16
- Product number
- 071922
- Product name
- 4-(2-Thiazolyl)phenol
- Purity
- 95+%
- Packaging
- 1g
- Price
- $347
- Updated
- 2021/12/16
- Product number
- OR913227
- Product name
- 4-(2-Thiazolyl)phenol
- Purity
- 95%
- Packaging
- 5g
- Price
- $395
- Updated
- 2021/12/16
4-(2-THIAZOLYL)PHENOL Chemical Properties,Usage,Production
Synthesis
27088-84-2
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
4-(2-THIAZOLYL)PHENOL Preparation Products And Raw materials
Raw materials
Preparation Products
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