1-Phenyl-o-carborane

1-Phenyl-o-carborane (CAS: 16390-61-7) is an organoboron compound, specifically an ortho-carborane (1,2-dicarba-closo-dodecaborane) derivative with a phenyl group (-C6H5) substituted at the 1-position of the ortho-carborane cage structure. Its molecular formula is C8B10H14, with a molecular weight of 202.32. It is a stable crystalline solid with unique carborane cage stability and aromatic ring characteristics, and is widely used as a key intermediate in organic synthesis, pharmaceutical, material and fine chemical fields.

1-Phenyl-o-carborane, 1-Phenyl-1,2-dicarba-closo-dodecaborane, Phenyl-o-carborane, 1-Phenylorthocarborane, 1-Phenyl-1,2-dicarba-closo-dodecaborane, (1,2-Dicarba-closo-dodecaboran-1-yl) benzene

1. Pharmaceutical Intermediates: 1-Phenyl-o-carborane (CAS: 16390-61-7) is an important intermediate in the synthesis of pharmaceutical compounds, especially in the research and development of anti-tumor drugs and boron neutron capture therapy (BNCT) agents, relying on its carborane cage structure to provide boron-rich properties and its phenyl group to enhance compatibility with organic drug molecules. 2. Material Intermediates: It is applied in the preparation of functional materials such as high-performance polymers, resin modifiers, optoelectronic materials and corrosion-resistant coatings. The carborane cage structure improves the material’s thermal stability and chemical resistance, while the phenyl group enhances the material’s compatibility with organic monomers. 3. Fine Chemicals: 1-Phenyl-o-carborane (CAS: 16390-61-7) serves as an intermediate in the synthesis of fine chemicals such as organic boron reagents, specialty dyes and analytical standards. Its unique structure (combining carborane cage and phenyl group) makes it suitable for specialized organic synthesis and analytical applications. 4. Chemical Research: It is widely used as a standard reagent and research tool in organoboron chemistry, carborane chemistry and synthetic chemistry research, facilitating the study of carborane cage reaction mechanisms, the development of new boron-containing organic compounds and the optimization of synthetic routes.

≥98%

C8B10H14

202.32

Store in a cool, dry and well-ventilated place, away from heat, open flame and direct sunlight, sealed tightly to prevent oxidation and light-induced decomposition; keep away from strong oxidants and reducing agents; avoid exposure to moisture

White to off-white crystalline powder

1.26 g/cm3 (at 25 °C, approx.)