Technical Parameters
Description
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China Factory 2-Naphthaleneboronic acid-d7丨CAS 1453542-02-3
Chemical Identifiers
| InChI | InChI=1S/C10H9BO2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7,12-13H/i1D,2D,3D,4D,5D,6D,7D |
| InChI Key | KPTRDYONBVUWPD-GSNKEKJESA-N |
| Smiles | [2H]C1=C(C(=C2C(=C(C(=C(C2=C1[2H])[2H])[2H])B(O)O)[2H])[2H])[2H] |
| EC No. | |
| MDL No. | |
| PubChem CID | 142716265 |
Applications
Deuterium Labeling and Mechanistic Studies
The seven deuterium atoms provide an isotopic label within the naphthalene framework. This feature can help researchers investigate isotope effects, reaction mechanisms, and chemical transformations. The boronic acid functionality also enables incorporation of the labeled aromatic unit into a variety of target molecules.
Pharmaceutical Research and Drug Discovery
Naphthalene-containing structures are investigated in medicinal chemistry and drug discovery. This deuterated intermediate may support the preparation of labeled analogues and aromatic derivatives for molecular design, structure–activity relationship studies, and early-stage pharmaceutical research, depending on the target compound.
Organic Synthesis and Cross-Coupling Reactions
The boronic acid group is widely used in Suzuki–Miyaura cross-coupling reactions with suitable organic halides. 2-Naphthaleneboronic acid-d7 can serve as a coupling partner for synthesizing deuterium-labeled biaryl compounds and other substituted aromatic derivatives, enabling further exploration of complex molecular architectures.
Materials Science and Organic Electronics
Naphthalene derivatives are important structural components in research on conjugated molecules and functional organic materials. 2-Naphthaleneboronic acid-d7 can be used as a building block for preparing deuterated aromatic compounds for investigations into molecular structure, photophysical behavior, and material properties.

