(5-Isopropoxy-3-pyridinyl)boronic acid

Basic Information

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CAS Number

850991-41-2

Molecular Formula

C8H12BNO3

Molecular Weight

181 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Ethers

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Basic Physical Properties

SMILES

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B(C1=CC(=CN=C1)OC(C)C)(O)O

InChI

InChI=1S/C8H12BNO3/c1-6(2)13-8-3-7(9(11)12)4-10-5-8/h3-6,11-12H,1-2H3

InChIKey

XQHUPBAXLPBXOT-UHFFFAOYSA-N

LogP

-0.45140000000000013

Topological Polar Surface Area

62.58 Å²

Hydrogen Bond Donor/Acceptor

2 / 4

Complexity

154

Synonyms & References

English

DTXSID40725467
5-isopropoxypyridin-3-ylboronic acid
CS-0046203
5-Isopropoxypyridine-3-boronic acid
(5-Isopropoxypyridin-3-yl)boronicacid
(5-propan-2-yloxypyridin-3-yl)boronic acid
[5-(PROPAN-2-YLOXY)PYRIDIN-3-YL]BORONIC ACID
(5-ISOPROPOXY-3-PYRIDYL)BORONIC ACID
850991-41-2
AKOS013525258
5-(ISOPROPOXY)PYRIDINE-3-BORONIC ACID
Boronic acid, [5-(1-methylethoxy)-3-pyridinyl]-
{5-[(Propan-2-yl)oxy]pyridin-3-yl}boronic acid
MFCD15529675
(5-Isopropoxy-3-pyridinyl)boronic acid
XQHUPBAXLPBXOT-UHFFFAOYSA-N
SCHEMBL2083713
D71488
EN300-251446
PS-13049
J-517651
5-Isopropoxy-3-pyridinylboronic acid
(5-Isopropoxypyridin-3-yl)boronic acid
(5-isopropoxypyridin-3-yl)boronic acid

MDL Number

MFCD15529675

FAQ

What are the physical and chemical properties of (5-Isopropoxy-3-pyridinyl)boronic acid (CAS: 850991-41-2)?

(5-Isopropoxy-3-pyridinyl)boronic acid has a crystalline form and a molecular weight of approximately 245.25 g/mol. It is slightly soluble in water and has good solubility in organic solvents. This compound is known for its reactivity in boronate ester formation and is stable under normal storage conditions.

How is (5-Isopropoxy-3-pyridinyl)boronic acid (CAS: 850991-41-2) typically synthesized?

(5-Isopropoxy-3-pyridinyl)boronic acid is typically synthesized via a protected pyridine route, where a protected pyridine derivative is reacted with boronic acid followed by deprotection. The reaction yields a high percentage of the desired product, with selectivity towards the boronic acid ester formation.

What industries use (5-Isopropoxy-3-pyridinyl)boronic acid (CAS: 850991-41-2)?

(5-Isopropoxy-3-pyridinyl)boronic acid is widely used in pharmaceuticals for drug synthesis, particularly in the development of boronate esters. It also finds applications in polymers for functionalization and in sensors for reactivity monitoring. In electronics, it is used in semiconductor manufacturing for specific chemical processes.

What precautions should be taken when handling (5-Isopropoxy-3-pyridinyl)boronic acid (CAS: 850991-41-2)?

When handling (5-Isopropoxy-3-pyridinyl)boronic acid, it is important to wear appropriate personal protective equipment (PPE), including gloves and safety glasses. Work in a well-ventilated area or fume hood to minimize inhalation risks. Follow standard laboratory safety protocols and consult the Safety Data Sheet (SDS) for specific handling and disposal instructions.