4-(Bromomethyl)-2,5-dimethyl-1,3-oxazole
95%
- Product Code: 130830
CAS:
857283-61-5
| Molecular Weight: | 190.04 g./mol | Molecular Formula: | C₆H₈BrNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29054829 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Sealed, Inert Gas |
Product Description:
Used primarily as a versatile intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. Its reactive bromomethyl group allows easy alkylation or substitution reactions, making it valuable for constructing complex molecules. Commonly employed in the preparation of heterocyclic compounds, it facilitates the introduction of the 2,5-dimethyloxazole moiety into target structures. This feature is exploited in drug discovery for modifying bioactive molecules, enhancing their metabolic stability or binding affinity. Also utilized in materials science for synthesizing functional organic materials due to the oxazole ring’s electronic properties. Its ability to act as a building block in cross-coupling reactions further extends its utility in developing new chemical entities.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $3,298.31 |
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4-(Bromomethyl)-2,5-dimethyl-1,3-oxazole
Used primarily as a versatile intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. Its reactive bromomethyl group allows easy alkylation or substitution reactions, making it valuable for constructing complex molecules. Commonly employed in the preparation of heterocyclic compounds, it facilitates the introduction of the 2,5-dimethyloxazole moiety into target structures. This feature is exploited in drug discovery for modifying bioactive molecules, enhancing their metabolic stability or binding affinity. Also utilized in materials science for synthesizing functional organic materials due to the oxazole ring’s electronic properties. Its ability to act as a building block in cross-coupling reactions further extends its utility in developing new chemical entities.
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