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762262-09-9

762262-09-9 Structure

762262-09-9 Structure
IdentificationBack Directory
[Name]

2-Methoxypyridne-4-boronic acid
[CAS]

762262-09-9
[Synonyms]

4-Borono-2-methoxypyridine
2-Methoxypyridne-4-boronic acid
2-Methoxypyridin-4-boronic acid
2-Methoxypridine-4-boronic acid
2-Methoxy-4-pyridylboronic Acid
2-Methoxy-4-pyridineboronic acid
2-METHOXYPYRIDINE-4-BORONIC ACID
2-METHOXYPYRIDIN-4-YLBORONIC ACID
2-METHOXY-4-PYRIDINYLBORONIC ACID
(2-Methoxypyridin-4-yl)boronicaci
2-METHOXY-4-PYRIDINE-4-BORONIC ACID
2-Methoxyl-4-pyridine boronic ester
2-Methoxypyridine-4-boronic acid 97%
2-Methoxypyridine-4-boronic acid ,97%
Boronic acid, B-(2-methoxy-4-pyridinyl)-
REF DUPL: 2-Methoxypyridine-4-boronic acid
Boronic acid, (2-methoxy-4-pyridinyl)- (9CI)
2-Methoxypyridne-4-boronic acid ISO 9001:2015 REACH
2-Methoxypyridine-4-boronicAcid(containsvaryingamountsofAnhydride)>
2-Methoxypyridine-4-boronic Acid (contains varying amounts of Anhydride)
[Molecular Formula]

C6H8BNO3
[MDL Number]

MFCD07368877
[MOL File]

762262-09-9.mol
[Molecular Weight]

152.94
Questions And AnswerBack Directory
[Synthesis]

2-Methoxypyridne-4-boronic acid is an important intermediate in the synthesis of N-type calcium ion channel inhibitors. It can be synthesized from readily available and inexpensive 4-bromopyridine via oxidation, nitration, substitution, reduction, and boronization reactions. The specific synthetic route is shown in the figure below.

Synthetic Route of 2-Methoxypyridne-4-boronic acid

Chemical PropertiesBack Directory
[Boiling point ]

325.7±52.0 °C(Predicted)
[density ]

1.24±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[form ]

powder to crystal
[pka]

7.11±0.10(Predicted)
[color ]

White to Light yellow to Light orange
[InChI]

InChI=1S/C6H8BNO3/c1-11-6-4-5(7(9)10)2-3-8-6/h2-4,9-10H,1H3
[InChIKey]

DHQMUJSACXTPEA-UHFFFAOYSA-N
[SMILES]

B(C1C=CN=C(OC)C=1)(O)O
Hazard InformationBack Directory
[Chemical Properties]

White powder
[Uses]

2-?Methoxypyridine-?4-?boronic Acid is a coupling reagent used in the synthesis of effacacious pyrrolopyridazines used as JAK1/3 inhibitors.
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

37/38-41-36/37/38
[Safety Statements ]

26-39-36
[Hazard Note ]

Irritant
[HS Code ]

29339900
Spectrum DetailBack Directory
[Spectrum Detail]

2-Methoxypyridne-4-boronic acid(762262-09-9)1HNMR
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