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2-CHLORO-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIDINE CAS:444120-94-9
2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a boron-containing organic compound notable for its unique structure, which includes a chloro-substituted pyridine ring and a dioxaborolane moiety. The presence of the dioxaborolane enhances the stability and reactivity of the compound in various chemical reactions, particularly in cross-coupling processes like Suzuki-Miyaura reactions. This compound serves as a valuable building block in organic synthesis, contributing to the development of complex molecules used in pharmaceuticals and agrochemicals, making it an important player in contemporary synthetic chemistry.
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5-Chloro-2-fluoropyridin-3-ylboronic acid CAS:937595-70-5
5-Chloro-2-fluoropyridin-3-ylboronic acid is a boron-containing compound characterized by a pyridine ring with chlorine and fluorine substituents at the fifth and second positions, respectively, along with a boronic acid functional group (-B(OH)₂) at the third position. Its molecular formula is C5H4ClFBN2O2. This compound is notable for its utility in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, making it an important building block for creating complex organic structures with diverse biological activities.
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![2-METHOXY-3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE CAS:532391-31-4](https://cdn.globalso.com/xindaobiotech/2QGOH2R49Y37X8W8E88O4D73.png)
2-METHOXY-3-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE CAS:532391-31-4
2-Methoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-pyridine is a boron-containing organic compound that features a pyridine ring substituted with a methoxy group and a dioxaborolane moiety. The inclusion of the dioxaborolane structure enhances the molecule’s stability and reactivity in various synthetic reactions. This compound is significant in organic synthesis, particularly for its role in cross-coupling reactions, such as Suzuki-Miyaura reactions. Its unique structural characteristics allow it to serve as a versatile building block for the development of complex organic molecules, including pharmaceuticals and agrochemicals, making it an important compound in modern synthetic chemistry.
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![3-FLUORO-5-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)PYRIDINE CAS:719268-92-5](https://cdn.globalso.com/xindaobiotech/HSUS81DS80Y35NTEZTU357.png)
3-FLUORO-5-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)PYRIDINE CAS:719268-92-5
3-Fluoro-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridine is a boron-containing organic compound characterized by the presence of a fluorine atom on the pyridine ring and a dioxaborolane substituent. This unique structure enhances its reactivity and stability, making it a valuable intermediary in various synthetic applications. Its incorporation into cross-coupling reactions, such as Suzuki-Miyaura reactions, allows for the efficient formation of carbon-carbon bonds. As a versatile building block, this compound plays a significant role in the development of pharmaceuticals, agrochemicals, and advanced materials, highlighting its importance in modern synthetic chemistry.
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1-Bromoadamantane CAS:768-90-1
1-Bromoadamantane is an organic compound belonging to the adamantane family, distinguished by the presence of a bromine atom attached to the first carbon of the adamantane structure. This compound retains the unique cage-like framework characteristic of adamantanes, contributing to its stability and distinctive chemical behavior. 1-Bromoadamantane is primarily utilized in organic synthesis and medicinal chemistry, serving as a key intermediate for producing various derivatives. Its reactivity with other functional groups makes it valuable in exploring new compounds with potential pharmaceutical applications.
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6-(4-morpholinyl)-3-pyridinylboronic acid CAS:904326-93-8
6-(4-Morpholinyl)-3-pyridinylboronic acid is a boron-containing compound that features a morpholine group attached to the pyridine ring at the sixth position and a boronic acid functional group. Its molecular formula is C11H14BNO2. This compound is valuable in organic synthesis, particularly in medicinal chemistry, where it serves as an important building block for the development of bioactive molecules. The unique structural characteristics impart specific reactivity, allowing it to participate in key reactions such as Suzuki-Miyaura cross-coupling, which facilitates the formation of carbon-carbon bonds in complex organic compounds.
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6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester CAS:485799-04-0
6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester is a boron-containing compound characterized by the presence of a morpholine moiety attached to the pyridine ring at the sixth position and a pinacol ester of boronic acid. This compound is notable for its utility in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The pinacol ester form enhances the stability and solubility of the boronic acid, facilitating its use in various chemical reactions, including Suzuki-Miyaura cross-coupling. Its unique structure allows for the synthesis of complex organic molecules with diverse biological activities.
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3-(DiMethylaMino)phenylboronic Acid Hydrochloride (contains varying aMounts of Anhydride) CAS:1256355-23-3
3-(Dimethylamino)phenylboronic acid hydrochloride is a boron-containing compound featuring a dimethylamino group attached to a phenyl ring at the meta position and a boronic acid functional group. The hydrochloride form enhances its solubility in water, making it suitable for various applications. This compound plays a crucial role in organic synthesis, particularly in medicinal chemistry, where it is used as a versatile building block for developing biologically active molecules. Its unique reactivity, especially in Suzuki-Miyaura cross-coupling reactions, enables the construction of complex organic structures important in pharmaceuticals and materials science.
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5-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-ylboronic acid CAS:475102-13-7
5-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-ylboronic acid is a specialized organic compound often used in pharmaceutical chemistry and synthetic organic research. The compound features an indole core, which is significant for bioactivity, along with a boronic acid functional group that facilitates cross-coupling reactions in Suzuki coupling processes. The tert-butoxycarbonyl (Boc) group provides a protective mechanism for the amine during synthesis, enhancing the compound’s stability. This structure makes it a pivotal intermediate in synthesizing various bioactive molecules, including potential drug candidates. Its unique properties enable chemists to manipulate and integrate it into diverse chemical frameworks.
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3-Methoxypyridine-5-boronic acid pinacol ester CAS:445264-60-8
3-Methoxypyridine-5-boronic acid pinacol ester is an important boron-containing compound widely used in organic synthesis. This compound features a pyridine ring with a methoxy substituent and a boronic acid moiety that is protected as a pinacol ester. The pinacol ester form enhances the stability of the boron functionality, making it more suitable for various coupling reactions, particularly in Suzuki-Miyaura cross-coupling. It serves as a versatile building block for synthesizing complex molecules, including pharmaceuticals and agrochemicals, due to its ability to facilitate carbon-carbon bond formation and further functional transformations.
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Ethyl 2-bromoheptanoate CAS:5333-88-0
Ethyl 2-bromoheptanoate is a halogenated ester characterized by a bromine atom attached to the second carbon of a seven-carbon heptanoate chain, with an ethyl group as the alcohol component. This compound belongs to the class of acyl bromides and serves as a valuable intermediate in organic synthesis due to its unique reactivity. The presence of both the bromo and ester functional groups allows for a variety of chemical transformations, making it useful in pharmaceutical chemistry, agrochemical applications, and the production of specialty chemicals. Its structure contributes to its distinctive properties and versatile applications.
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1,3-Dibromo-2-propanol CAS:96-21-9
1,3-Dibromo-2-propanol is a halogenated organic compound featuring two bromine atoms attached to the first and third carbon atoms of a three-carbon propanol backbone. The presence of a hydroxyl group (-OH) on the second carbon makes it a dihalogenated alcohol. This compound’s unique structure gives it distinct chemical reactivity and properties, making it an important intermediate in organic synthesis. It is primarily utilized in the preparation of various organic compounds and has applications in medicinal chemistry, agrochemicals, and the production of specialty chemicals due to its ability to engage in nucleophilic substitution reactions.
