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3-CYANOPYRIDIN-4-YLBORONIC ACID

Product Name
3-CYANOPYRIDIN-4-YLBORONIC ACID
CAS No.
874290-89-8
Chemical Name
3-CYANOPYRIDIN-4-YLBORONIC ACID
Synonyms
(3-Cyanopyridin-4-yl)boronic;3-Cyano-4-pyridineboronic Acid;3-CYANOPYRIDINE-4-BORONIC ACID;3-CYANOPYRIDIN-4-YLBORONIC ACID;3-cyano-4-pyridinyl boronic acid;3-Cyanopyridine-4-boronic acid ,95%;B-(3-cyano-4-pyridinyl)-Boronic acid;Boronic acid, B-(3-cyano-4-pyridinyl)-
CBNumber
CB2837347
Molecular Formula
C6H5BN2O2
Formula Weight
147.93
MOL File
874290-89-8.mol
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3-CYANOPYRIDIN-4-YLBORONIC ACID Property

Boiling point:
407.9±55.0 °C(Predicted)
Density 
1.34±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
7.04±0.58(Predicted)
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Safety

Hazard Codes 
Xn
Risk Statements 
22
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P330Rinse mouth.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Biosynth Carbosynth
Product number
FC151984
Product name
3-Cyanopyridine-4-boronicacid
Packaging
10mg
Price
$66
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC151984
Product name
3-Cyanopyridine-4-boronicacid
Packaging
25mg
Price
$120
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC151984
Product name
3-Cyanopyridine-4-boronicacid
Packaging
50mg
Price
$200
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC151984
Product name
3-Cyanopyridine-4-boronicacid
Packaging
100mg
Price
$300
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC151984
Product name
3-Cyanopyridine-4-boronicacid
Packaging
250mg
Price
$535
Updated
2021/12/16
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3-CYANOPYRIDIN-4-YLBORONIC ACID Chemical Properties,Usage,Production

Synthesis

100-54-9

5419-55-6

874290-89-8

Under nitrogen protection, 300 g of anhydrous tetrahydrofuran was added to the reaction flask with stirring turned on, followed by the addition of 12 g of 3-cyanopyridine and cooling of the system to -30°C. The reaction was carried out under nitrogen protection. Slowly 70 mL of 2.0 M n-butyllithium solution was added dropwise. After stirring for 30 minutes, 1,4,7,10-tetramethyl-1,4,7,10-tetraazacyclododecane solution was added slowly dropwise. After 2 hours of reaction, 41 mL of triisopropyl borate was slowly added dropwise. Stirring was continued at -30°C for 1 hour, then slowly warmed to room temperature and stirred for 1 hour. To the reaction mixture was added 400 g of concentrated hydrochloric acid and stirred for 1 hour for hydrolysis. After completion of the reaction, the reaction was left to partition and the organic layer was washed with water three times (100 g each). The aqueous layer was combined and extracted once with 100 mL of petroleum ether. The organic layers were combined, dried with 50 g of anhydrous sodium sulfate and filtered. The filtrate was concentrated to dryness to give 14 g of 3-cyano-4-pyridineboronic acid.

References

[1] Patent: CN102718785, 2016, B. Location in patent: Paragraph 0040; 0041

3-CYANOPYRIDIN-4-YLBORONIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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874290-89-8, 3-CYANOPYRIDIN-4-YLBORONIC ACIDRelated Search:


  • 3-CYANOPYRIDINE-4-BORONIC ACID
  • 3-CYANOPYRIDIN-4-YLBORONIC ACID
  • 3-Cyanopyridine-4-boronic acid ,95%
  • B-(3-cyano-4-pyridinyl)-Boronic acid
  • 3-cyano-4-pyridinyl boronic acid
  • Boronic acid, B-(3-cyano-4-pyridinyl)-
  • 3-Cyano-4-pyridineboronic Acid
  • (3-Cyanopyridin-4-yl)boronic
  • 874290-89-8