2-(4-METHOXY-PHENYL)-BENZOOXAZOLE
- Product Name
- 2-(4-METHOXY-PHENYL)-BENZOOXAZOLE
- CAS No.
- 838-34-6
- Chemical Name
- 2-(4-METHOXY-PHENYL)-BENZOOXAZOLE
- Synonyms
- 2-(4-METHOXY-PHENYL)-BENZOOXAZOLE;Benzoxazole, 2-(4-methoxyphenyl)-;2-(4-Methoxyphenyl)benzo[d]oxazole;2-(4-Methoxyphenyl)-1,3-benzoxazole;Benzoxazole, 2-(4-Methoxyphenyl)-Benzoxazole, 2-(p-Methoxyphenyl)- (6CI,7CI,8CI)
- CBNumber
- CB52463707
- Molecular Formula
- C14H11NO2
- Formula Weight
- 225.24
- MOL File
- 838-34-6.mol
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
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
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
- PH004300
- Product name
- 2-(4-methoxyphenyl)-1,3-benzoxazole
- Purity
- AldrichCPR
- Packaging
- 1mg
- Price
- $134
- Updated
- 2023/06/20
- Product number
- M3709
- Product name
- 2-(4-Methoxyphenyl)benzo[d]oxazole
- Purity
- min. 95.0 %
- Packaging
- 100MG
- Price
- $124
- Updated
- 2026/03/19
- Product number
- 176433
- Product name
- 2-(4-Methoxyphenyl)-1,3-benzoxazole
- Packaging
- 1g
- Price
- $316
- Updated
- 2021/12/16
- Product number
- CHM1035835
- Product name
- 2-(4-METHOXY-PHENYL)-BENZOOXAZOLE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $496.01
- Updated
- 2021/12/16
- Product number
- 176433
- Product name
- 2-(4-Methoxyphenyl)-1,3-benzoxazole
- Packaging
- 5g
- Price
- $810
- Updated
- 2021/12/16
2-(4-METHOXY-PHENYL)-BENZOOXAZOLE Chemical Properties,Usage,Production
Synthesis Reference(s)
Tetrahedron, 53, p. 457, 1997 DOI: 10.1016/S0040-4020(96)01009-5
Synthesis
The synthesis of 2-(4-methoxyphenyl)benzo[d]oxazole typically involves the condensation reaction of 2-aminophenol with a 4-methoxybenzoic acid derivative (e.g., an acid, ester, or aldehyde) under various conditions, including thermal cyclization, microwave irradiation, or the use of specific catalysts such as Lewis acids or palladium complexes, which promote the formation of the benzoxazole ring structure. A common conventional method is the direct cyclization reaction of 2-aminophenol with 4-methoxybenzoic acid, which usually requires high temperatures or dehydrating agents.
2-(4-METHOXY-PHENYL)-BENZOOXAZOLE Preparation Products And Raw materials
Raw materials
Preparation Products
2-(4-METHOXY-PHENYL)-BENZOOXAZOLE Suppliers
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