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1-naphthaleneboronic Acid-d7丨CAS 1000869-26-0

1-naphthaleneboronic Acid-d7丨CAS 1000869-26-0
Product Introduction:
CAS No.: 1000869-26-0
Product Name: 1-naphthaleneboronic acid-d7
Molecular Formula: C10H9BO2
Molecular Weight: 179.03
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Technical Parameters
Description

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Custom Synthesis 1-naphthaleneboronic acid-d7丨CAS 1000869-26-0

 

1-Naphthaleneboronic acid-d7 is a deuterium-labeled aromatic boronic acid featuring a naphthalene ring system and a boronic acid functional group. With seven deuterium atoms incorporated into its molecular structure, this compound is a specialized building block for organic synthesis, isotope-labeling research, and the development of advanced functional molecules. Its boronic acid group provides a versatile reaction site for forming carbon–carbon bonds and preparing substituted aromatic compounds.

 

Chemical Identifiers

 

InChI InChI=1S/C10H9BO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7,12-13H/i1D,2D,3D,4D,5D,6D,7D
InChI Key HUMMCEUVDBVXTQ-GSNKEKJESA-N
Smiles [2H]C1=C(C(=C2C(=C(C(=C(C2=C1[2H])[2H])[2H])[2H])B(O)O)[2H])[2H]
EC No.  
MDL No.  
PubChem CID 140701541

 

 

 

Applications

 

Deuterium Labeling and Mechanistic Studies

The seven deuterium atoms provide an isotopic label within the naphthalene framework. This feature can support studies of isotope effects, reaction mechanisms, and chemical transformations, as well as the preparation of deuterium-labeled aromatic compounds for specialized research applications.

Pharmaceutical Research and Drug Discovery

Naphthalene-containing structures appear in a variety of biologically active compounds and medicinal chemistry research programs. This deuterated boronic acid may be used as a synthetic intermediate for preparing labeled analogues and exploring structure–activity relationships in early-stage drug discovery, depending on the target molecule.

Suzuki–Miyaura Cross-Coupling Reactions

Aromatic boronic acids are widely used in Suzuki–Miyaura cross-coupling reactions with suitable organic halides. 1-Naphthaleneboronic acid-d7 can serve as a deuterated coupling partner for introducing a labeled naphthalene unit into more complex molecular structures, supporting the synthesis of isotopically labeled biaryl compounds and functional aromatic derivatives.

Materials Science and Functional Aromatic Compounds

Naphthalene is an important structural motif in research on conjugated molecules and organic functional materials. 1-Naphthaleneboronic acid-d7 can be used to introduce a deuterated naphthalene unit into larger molecular architectures, supporting investigations into molecular structure and material properties.

 

 

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