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697739-22-3

2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Catalog#: AR003HPQ  |   CAS#: 697739-22-3  |   MDL#: MFCD08063106  |   MF: C12H17BClNO2  |   MW: 253.5329

Packsize Purity Price Availability Quantity
100mg 97% $11.00 Global Stock Buy Now Add To Cart
250mg 97% $22.00 Global Stock Buy Now Add To Cart
500mg 97% $39.00 Global Stock Buy Now Add To Cart
1g 97% $70.00 Global Stock Buy Now Add To Cart
5g 97% $260.00 Global Stock Buy Now Add To Cart
10g 97% $450.00 Global Stock Buy Now Add To Cart
25g 97% $918.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003HPQ
Chemical Name 2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
CAS Number 697739-22-3
Molecular Formula C12H17BClNO2
Molecular Weight 253.5329
MDL Number MFCD08063106
SMILES Cc1nc(Cl)cc(c1)B1OC(C(O1)(C)C)(C)C

2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure containing a boronate ester moiety makes it particularly valuable as a key building block in organic chemistry.In the realm of chemical synthesis, $name$ is frequently employed as a key reagent in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, enables the formation of carbon-carbon bonds between aryl or vinyl halides and boronic acids or boronate esters. By serving as the boronate component in this transformative process, $name$ facilitates the construction of complex organic molecules with high efficiency and selectivity.Moreover, the presence of the chloropyridine functionality in $name$ offers further synthetic utility, allowing for additional derivatization and diversification of the molecule. Through strategic manipulation of the chloro and boronic acid groups, chemists can access a wide array of structurally diverse compounds, making $name$ a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and materials science.In summary, the strategic incorporation of 2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, or $name$, in chemical synthesis enables the efficient construction of novel organic molecules with significant implications for drug discovery, materials development, and other fields of science and industry.
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Pyridine, 2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trifluoromethyl)-

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2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

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697739-22-3

2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

697739-22-3

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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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