6-Chloro-3-pyridinylboronic acid

97%

  • Product Code: 90957
  Alias:    6-Chloropyridine-3-boronic acid
  CAS:    444120-91-6
Molecular Weight: 157.36 g./mol Molecular Formula: C₅H₅BClNO₂
EC Number: MDL Number: MFCD03094998
Melting Point: 165 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of drugs targeting central nervous system disorders. It is also employed in the development of agrochemicals, such as insecticides and herbicides, due to its role in creating compounds that effectively control pests and weeds. In material science, it serves as a building block for organic electronic materials, contributing to the advancement of OLEDs and other optoelectronic devices. Additionally, it is utilized in cross-coupling reactions, such as Suzuki-Miyaura reactions, to form carbon-carbon bonds in organic synthesis, enabling the creation of complex molecules for research and industrial applications.
Product Specification:
Test Specification
Melting point 161-167
PURITYHPLC 97-100
PURITYNEUTRALIZATION TITRATION 97-100
APPEARANCE Yellow to brown powder
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿280.00
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1.000 10-20 days ฿320.00
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5.000 10-20 days ฿840.00
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25.000 10-20 days ฿3,680.00
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100.000 10-20 days ฿12,580.00
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6-Chloro-3-pyridinylboronic acid
Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of drugs targeting central nervous system disorders. It is also employed in the development of agrochemicals, such as insecticides and herbicides, due to its role in creating compounds that effectively control pests and weeds. In material science, it serves as a building block for organic electronic materials, contributing to the advancement of OLEDs and other optoelectronic devices. Additionally, it is utilized in cross-coupling reactions, such as Suzuki-Miyaura reactions, to form carbon-carbon bonds in organic synthesis, enabling the creation of complex molecules for research and industrial applications.
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