2-[1-(4-BROMOPHENYL)-1-METHYLETHYL]-4,4-DIMETHYL-4,5-DIHYDROOXAZOLINE

98%

Reagent Code: #146979
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CAS Number 192775-97-6

science Other reagents with same CAS 192775-97-6

blur_circular Chemical Specifications

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Weight 296.2 g/mol
Formula C₁₄H₁₈BrNO
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its brominated aromatic structure makes it suitable for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. The oxazoline ring acts as a directing group or chiral auxiliary in asymmetric synthesis, aiding in stereochemical control during carbon-carbon bond formation. It is also employed in the development of ligands for catalytic processes, enhancing reaction selectivity in metal-catalyzed transformations.

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inventory 5g
10-20 days ฿13,180.00

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2-[1-(4-BROMOPHENYL)-1-METHYLETHYL]-4,4-DIMETHYL-4,5-DIHYDROOXAZOLINE
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its brominated aromatic structure makes it suitable for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. The oxazoline ring acts as a directing group or chiral auxiliary in asymmetric synthesis, aiding in stereochemical control during carbon-carbon bond formation. It is also employed in the development of ligands for catalytic proce

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its brominated aromatic structure makes it suitable for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. The oxazoline ring acts as a directing group or chiral auxiliary in asymmetric synthesis, aiding in stereochemical control during carbon-carbon bond formation. It is also employed in the development of ligands for catalytic processes, enhancing reaction selectivity in metal-catalyzed transformations.

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