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9,9-Dimethyl-2-iodofluorene CAS:144981-85-1
9,9-Dimethyl-2-iodofluorene is a compound of interest in the field of organic chemistry and material science, renowned for its versatile applications in the synthesis of various organic compounds and functional materials. This molecule belongs to the fluorene family, characterized by a polycyclic aromatic structure that confers unique electronic and optical properties. The presence of a methyl group at the 9th position and an iodine atom at the 2nd position enhances the reactivity and tunability of 9,9-Dimethyl-2-iodofluorene, making it a valuable building block in organic synthesis.
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2′-Fluoroacetophenone CAS:445-27-2
2′-Fluoroacetophenone is a notable compound in the realm of organic chemistry, recognized for its diverse applications in synthetic organic chemistry and pharmaceutical research. With the fluorine atom positioned at the para position of the acetophenone framework, this molecule exhibits unique chemical properties that make it valuable for a range of synthetic purposes and medicinal chemistry endeavors. The presence of the fluorine substituent offers opportunities for exploring novel reactivity patterns, molecular transformations, and potential pharmacological activities. Understanding the structural features and chemical behavior of 2′-Fluoroacetophenone is essential for advancing research in organic synthesis, drug discovery, and medicinal chemistry.
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2-IODO-9H-FLUORENE CAS:2523-42-4
2-Iodo-9H-fluorene is a halogenated derivative of fluorene, a polycyclic aromatic hydrocarbon. With the chemical formula C₁₃H₉I, it consists of a fluorene core substituted with an iodine atom. This compound finds applications in organic synthesis, particularly in the preparation of various functionalized fluorene derivatives. The introduction of iodine imparts unique properties to the molecule, making it valuable in pharmaceuticals, materials science, and chemical research.
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9-Phenyl-9H-carbazol-3-ylboronic acid CAS:854952-58-2
9-Phenyl-9H-carbazol-3-ylboronic acid is a significant compound in the field of organic chemistry due to its versatile applications and structural properties. It belongs to the class of boronic acids, which are renowned for their utility in various synthetic processes, particularly in Suzuki-Miyaura cross-coupling reactions for constructing carbon-carbon bonds.
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9,10-Dibromoanthracene CAS:523-27-3
9,10-Dibromoanthracene is a notable compound that holds substantial significance in the realms of organic chemistry, materials science, and photochemistry. With bromine atoms attached to both the ninth and tenth positions of the anthracene core, this molecule exhibits distinct chemical properties that render it valuable for a range of synthetic applications and functional material design. The symmetrical placement of the bromine substituents on the anthracene framework offers unique opportunities for exploring reactivity patterns, molecular transformations, and optical properties. Understanding the structural features and chemical behavior of 9,10-Dibromoanthracene is essential for advancing research in organic synthesis, photoactive materials, and optoelectronic devices.
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9,9-Dimethyl-9H-fluoren-2-yl-boronic acid CAS:333432-28-3
9,9-Dimethyl-9H-fluoren-2-yl-boronic acid is a boronic acid derivative that holds significant importance in the field of organic synthesis and materials science. With its unique molecular structure and versatile reactivity, this compound has found widespread applications in various areas of research and industrial processes.
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9,9-Dimethyl-9H-2,7-diiodofluorene CAS:144981-86-2
9,9-Dimethyl-9H-2,7-diiodofluorene is a compound with significant relevance in organic chemistry due to its unique structural features and potential applications. With its distinctive substitution pattern, this compound offers intriguing possibilities for synthetic chemistry, material science, and pharmaceutical research.
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9,9-Dimethyl-9H-fluorene CAS:4569-45-3
9,9-Dimethyl-9H-fluorene is a polycyclic aromatic hydrocarbon (PAH) compound with a molecular formula C15H14. It is derived from fluorene by the addition of two methyl groups at the 9th position, resulting in increased steric hindrance and altered chemical properties. This modification affects its solubility, reactivity, and electronic properties, making it valuable in various applications such as organic electronics, materials science, and medicinal chemistry. Understanding its synthesis, structure-property relationships, and applications is crucial for harnessing its full potential in diverse fields.
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9-Bromoanthracene CAS:1564-64-3
9-Bromoanthracene is a compelling molecule that holds significant importance in the realm of organic chemistry and materials science. Featuring a bromine atom attached to the ninth carbon atom of the anthracene framework, this compound exhibits unique chemical properties that make it valuable for various synthetic applications and material design. The presence of both the aromatic anthracene core and the bromine substituent creates intriguing opportunities for exploring novel reactivity patterns, molecular transformations, and potential functionalization strategies. Understanding the structural characteristics and chemical behavior of 9-Bromoanthracene is crucial for advancing research in organic synthesis, molecular design, and material development.
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2,3-DIFLUOROETHOXYBENZENE CAS:121219-07-6
2,3-Difluoroethoxybenzene is a compound of interest in organic chemistry due to its unique structure and potential applications in synthesis and material science. With two fluorine atoms attached to the ethoxybenzene framework at the 2 and 3 positions, this molecule exhibits distinct chemical properties that make it valuable for various chemical reactions and functionalization strategies. The presence of the difluoroethoxy group offers opportunities for exploring novel reactivity patterns and molecular transformations, making it a versatile building block for designing new organic compounds and materials. Understanding the structural characteristics and chemical behavior of 2,3-Difluoroethoxybenzene is crucial for advancing research in organic synthesis, materials chemistry, and related fields.
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2-Bromo-9,9-dimethylfluorene CAS:28320-31-2
2-Bromo-9,9-dimethylfluorene is a derivative of fluorene, a polycyclic aromatic hydrocarbon consisting of two benzene rings fused together. With the substitution of a bromine atom at the 2-position and methyl groups at the 9-positions, it exhibits unique chemical properties compared to its parent compound.
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2,7-Dibromo-9,9-dimethylfluorene CAS:28320-32-3
2,7-Dibromo-9,9-dimethylfluorene is a compound of interest in organic chemistry due to its unique structural properties and potential applications. It belongs to the fluorene family, characterized by a fluorene core with bromine substituents at the 2 and 7 positions, along with dimethyl groups at the 9 position. This molecular arrangement imparts specific chemical and physical characteristics to the compound, making it valuable in various fields such as materials science, pharmaceuticals, and organic electronics. Understanding its synthesis, properties, and reactivity is crucial for leveraging its potential in diverse applications.
