1-Naphthaleneboronic acid-d7
Based on 1 Customer Validation
1-Naphthaleneboronic acid-d7 is the deuterated-labeled 1-Naphthaleneboronic acid (HY-78494). 1-Naphthaleneboronic acid is a biochemical reagent that can serve as a starting material or reaction reagent for chemical synthesis. 1-Naphthaleneboronic acid mainly introduces its naphthalene ring into other scaffolds through Suzuki-Miyaura cross-coupling or Friedel-Crafts alkylation reactions, thereby synthesizing target products with specific functions such as fluorescence imaging, photodynamic therapy targeting, or affinity adsorption. 1-Naphthaleneboronic acid can be used in research on photosensitizers and the synthesis of hypercrosslinked polymers with boronic acid affinity.
For research use only. We do not sell to patients.
- CAS No.: 1000869-26-0
- Formula: C10H2D7BO2
- Molecular Weight:179.03
-
Storage:
4°C, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
Biological Activity
Description
Application
1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Chemical Information
-
CAS No. 1000869-26-0
-
Unlabeled CAS 13922-41-3
-
Appearance Solid
-
Molecular Weight 179.03
-
Formula C10H2D7BO2
-
SMILES
[2H]C1=C([2H])C([2H])=C([2H])C2=C([2H])C([2H])=C([2H])C(B(O)O)=C12
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
4°C, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
Purity & Documentation
-
Data Sheet (293 KB)
-
SDS (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
-
Handling Instructions (2659 KB)
References
[6]. Tan YJ, et al. Galloyl esters of trans-stilbenes are inhibitors of FASN with anticancer activity on non-small cell lung cancer cells. European journal of medicinal chemistry. 2019 Nov 15;182:111597. [Content Brief]
[9]. Singh S, et al. Discovery of a novel series of N-hydroxypyridone derivatives protecting astrocytes against hydrogen peroxide-induced toxicity via improved mitochondrial functionality. Bioorganic & medicinal chemistry. 2017 Feb 15;25(4):1394-1405. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- 1-Naphthaleneboronic acid-d7
- 1000869-26-0
- Isotope-Labeled Compounds
- Biochemical Assay Reagents
- Arthrobacter nicotinovorans
- G-quadruplex hydrogel
- Suzuki-Miyaura cross-coupling
- boronate ester
- hypercrosslinked polymers
- monooxygenation
- naphthol
- organic synthesis
- oxidation
- thixotropic recovery
- Inhibitor
- inhibitor
- inhibit