5-METHYLBENZOXAZOLE
5-METHYLBENZOXAZOLE Basic information
- Product Name:
- 5-METHYLBENZOXAZOLE
- Synonyms:
-
- 5-METHYLBENZOXAZOLE
- 5-METHYL-1,3-BENZOXAZOLE
- 5-Methylbenzoxazole, 99.5+%
- 5-Methyl-benzooxazole
- 5-Methylbenzo[d]oxazole
- 5-Methylbenzoxazole 97%
- 5-Methylbenzoxazole>
- Benzoxazole, 5-methyl-
- CAS:
- 10531-78-9
- MF:
- C8H7NO
- MW:
- 133.15
- Product Categories:
-
- Oxazoles, Isoxazoles & Benzoxazoles
- Oxazole&Isoxazole
- Oxazoles, Isoxazoles & Benzoxazoles
- Mol File:
- 10531-78-9.mol
5-METHYLBENZOXAZOLE Chemical Properties
- Melting point:
- 41-44 °C
- Boiling point:
- 96 °C / 15mmHg
- Density
- 1.1475 (rough estimate)
- refractive index
- 1.5320 (estimate)
- Flash point:
- 87℃
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 2.66±0.10(Predicted)
- color
- White to Green to Brown
- CAS DataBase Reference
- 10531-78-9(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,C,Xn
- Risk Statements
- 36/37/38-37/38-36-34-20/21/22-41-22
- Safety Statements
- 37/39-26-45-36/37/39-27-39-36
- WGK Germany
- 1
- HS Code
- 29349990
5-METHYLBENZOXAZOLE Usage And Synthesis
Chemical Properties
YELLOW TO BROWN CRYSTALLINE SOLID
Synthesis
122-51-0
95-84-1
10531-78-9
GENERAL METHOD: Triethyl orthoformate (1.1 mmol) and o-amino-p-toluol (1 mmol) were mixed and p-toluenesulfonic acid (TSA, 1 mol%) was added as a catalyst. The reaction mixture was stirred at 80-90 °C for an appropriate time depending on the course of the reaction (cf. Table 4). After completion of the reaction (monitored by TLC), the reaction mixture was diluted with chloroform (10 mL) and the catalyst was removed by filtration. The final product 5-methylbenzazole was purified by column chromatography.
References
[1] Monatshefte fur Chemie, 2011, vol. 142, # 1, p. 87 - 91
[2] Combinatorial Chemistry and High Throughput Screening, 2013, vol. 16, # 8, p. 618 - 627
[3] Chemical Communications, 2014, vol. 50, # 73, p. 10661 - 10664
[4] Monatshefte fur Chemie, 2007, vol. 138, # 7, p. 663 - 667
[5] Comptes Rendus Chimie, 2013, vol. 16, # 11, p. 1029 - 1034
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