6-(Bromomethyl)-4-chloroquinazoline

95%

Reagent Code: #49508
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CAS Number 153436-68-1

science Other reagents with same CAS 153436-68-1

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Weight 257.5143 g/mol
Formula C₉H₆BrClN₂
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MDL Number MFCD09701986
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6-(Bromomethyl)-4-chloroquinazoline is primarily utilized in organic synthesis as a versatile intermediate for constructing more complex quinazoline derivatives. Its reactive bromomethyl group allows for nucleophilic substitution reactions, making it valuable in the development of pharmaceuticals, particularly in the synthesis of kinase inhibitors and anticancer agents. The compound is also employed in the preparation of biologically active molecules targeting various diseases, leveraging its ability to introduce functional groups at specific positions on the quinazoline core. Additionally, it serves as a key building block in medicinal chemistry research for designing and optimizing drug candidates with enhanced therapeutic properties.

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inventory 100mg
10-20 days ฿5,517.00

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6-(Bromomethyl)-4-chloroquinazoline
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6-(Bromomethyl)-4-chloroquinazoline is primarily utilized in organic synthesis as a versatile intermediate for constructing more complex quinazoline derivatives. Its reactive bromomethyl group allows for nucleophilic substitution reactions, making it valuable in the development of pharmaceuticals, particularly in the synthesis of kinase inhibitors and anticancer agents. The compound is also employed in the preparation of biologically active molecules targeting various diseases, leveraging its ability to int
6-(Bromomethyl)-4-chloroquinazoline is primarily utilized in organic synthesis as a versatile intermediate for constructing more complex quinazoline derivatives. Its reactive bromomethyl group allows for nucleophilic substitution reactions, making it valuable in the development of pharmaceuticals, particularly in the synthesis of kinase inhibitors and anticancer agents. The compound is also employed in the preparation of biologically active molecules targeting various diseases, leveraging its ability to introduce functional groups at specific positions on the quinazoline core. Additionally, it serves as a key building block in medicinal chemistry research for designing and optimizing drug candidates with enhanced therapeutic properties.
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