(4-Formyl-1-naphthyl)boronic acid

Basic Information

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CAS Number

332398-52-4

Molecular Formula

C11H9BO3

Molecular Weight

200 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Aldehydes

Fine Chemicals Dyes and Pigments Organic Dyes

Fine Chemicals Surfactants Anionic Surfactants

Basic Physical Properties

Melting Point

230°C

SMILES

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B(C1=CC=C(C2=CC=CC=C12)C=O)(O)O

InChI

InChI=1S/C11H9BO3/c13-7-8-5-6-11(12(14)15)10-4-2-1-3-9(8)10/h1-7,14-15H

InChIKey

KBHGTTWVFRLPRO-UHFFFAOYSA-N

LogP

0.33209999999999995

Topological Polar Surface Area

57.53 Å²

Hydrogen Bond Donor/Acceptor

2 / 3

Complexity

232

Synonyms & References

English

CS-0014226
Boronic acid, (4-formyl-1-naphthalenyl)-
BS-32287
332398-52-4
(4-Formyl-1-naphthalene)boronic acid
DTXSID80378451
4-Formyl-1-naphthaleneboronicacid
C11H9BO3
(4-formyl-1-naphthyl)boronic acid
MFCD01632205
A821687
AKOS004116435
D95611
(4-formylnaphthalen-1-yl)boronicAcid
SCHEMBL257891
4-formylnaphthalen-1-ylboronic acid
AB09475
4-Formylnaphthalene-1-boronic acid
(4-formylnaphthalen-1-yl)boronic Acid
FT-0690442
(4-Formylnaphthalen-1-yl)boronic acid
Boronicacid, B-(4-formyl-1-naphthalenyl)-
(4-FORMYL-1-NAPHTHALENE)BORONIC ACID
4-formyl-1-naphthylboronic acid
4-formylnaphthylboronic acid

MDL Number

MFCD01632205

FAQ

What are the physical and chemical properties of (4-Formyl-1-naphthyl)boronic acid (CAS: 332398-52-4)?

(4-Formyl-1-naphthyl)boronic acid is a crystalline solid with a molecular weight of approximately 262.3 g/mol. It has limited water solubility and is more soluble in organic solvents. The compound exhibits typical reactivity of boronic acids, undergoing reactions such as Suzuki coupling with various aryl halides. Its solubility in common solvents and reactivity make it suitable for various synthetic applications.

How is (4-Formyl-1-naphthyl)boronic acid (CAS: 332398-52-4) typically synthesized?

(4-Formyl-1-naphthyl)boronic acid is often prepared via a condensation reaction between 1-naphthylboronic acid and formaldehyde, followed by a reduction step to form the boronic acid. This synthesis typically involves the use of a suitable reducing agent like sodium borohydride to achieve the desired product. The reaction is carried out under mild conditions to ensure high selectivity and yield.

What industries use (4-Formyl-1-naphthyl)boronic acid (CAS: 332398-52-4)?

(4-Formyl-1-naphthyl)boronic acid finds applications in pharmaceuticals, where it can serve as a building block in the synthesis of complex molecules. It is also used in polymer chemistry for functionalizing polymers and in semiconductor manufacturing for specific applications. Its reactivity and functionality make it valuable in these industries for creating advanced materials and products.

What precautions should be taken when handling (4-Formyl-1-naphthyl)boronic acid (CAS: 332398-52-4)?

When handling (4-Formyl-1-naphthyl)boronic acid, it is important to wear appropriate personal protective equipment (PPE), including gloves, goggles, and a laboratory coat. Work under a fume hood to prevent inhalation of any vapors. Spills should be carefully cleaned up using suitable absorbents, and the area should be well-ventilated. Always consult the Safety Data Sheet (SDS) for detailed handling and disposal information.