CAS 33626-98-1
:2-Naphthalenecarboxylic acid, 6-bromo-, methyl ester
Description:
2-Naphthalenecarboxylic acid, 6-bromo-, methyl ester, also known by its CAS number 33626-98-1, is an organic compound characterized by its naphthalene structure substituted with a carboxylic acid group and a bromine atom at the 6-position, along with a methyl ester functional group. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents such as ethanol and acetone, but may have limited solubility in water due to its hydrophobic naphthalene ring. The presence of the bromine atom introduces notable reactivity, making it a useful intermediate in various organic synthesis reactions, including electrophilic aromatic substitution. Its ester functionality can undergo hydrolysis, transesterification, or other reactions typical of carboxylic acid derivatives. The compound may exhibit biological activity, and its derivatives are often explored in medicinal chemistry for potential therapeutic applications. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.
Formula:C12H9BrO2
InChI:InChI=1S/C12H9BrO2/c1-15-12(14)10-3-2-9-7-11(13)5-4-8(9)6-10/h2-7H,1H3
InChI key:InChIKey=JEUBRLPXJZOGPX-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=CC2=C(C=C(Br)C=C2)C=C1
Synonyms:- 2-Bromo-6-methoxycarbonylnaphthalene
- 2-Naphthalenecarboxylic acid, 6-bromo-, methyl ester
- 2-Naphthoic acid, 6-bromo-, methyl ester
- 6-Bromo-2-naphthoic acid methyl ester
- 6-Bromonaphthalene-2-carboxylic acid methyl ester
- Methyl 6-(3-benzyl-4-((2-methoxyethoxy)methoxy)phenyl)-2-naphthoate
- Methyl 6-Bromonaphthalene-2-Carboxylate
- Methyl 6-bromo-2-naphthoate
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Found 12 products.
Methyl 6-Bromo-2-naphthoate
CAS:Formula:C12H9BrO2Purity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:265.11Methyl 6-bromo-2-naphthoate, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C12H9BrO2Purity:98%Color and Shape:White, PowderMolecular weight:265.11Adapalene Related Compound A (Methyl 6-bromo-2-naphthoate)
CAS:Aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacid and their derivatives, nesoiFormula:C12H9BrO2Color and Shape:White Off-White Tan PowderMolecular weight:263.97859Methyl 6-bromo-2-naphthoate
CAS:Formula:C12H9BrO2Purity:98%Color and Shape:SolidMolecular weight:265.1027Methyl 6-Bromo-2-naphthoate
CAS:<p>Methyl 6-Bromo-2-naphthoate</p>Purity:98%Molecular weight:265.10g/molAdapalene USP Related Compound A
CAS:Controlled ProductFormula:C12H9BrO2Color and Shape:NeatMolecular weight:265.10Methyl 6-Bromo-2-napthoate
CAS:Controlled Product<p>Impurity Adapalene USP Related Compound A<br>Applications Methyl 6-Bromo-2-napthoate (Adapalene USP Related Compound A) is used in the synthesis of Adapalene, a retinoid specific for RARβ and RARγ receptors.<br>References Milanese, A. et al.: Bioorg. Chem., 9, 151 (2011);<br></p>Formula:C12H9BrO2Color and Shape:NeatMolecular weight:265.10Methyl 6-bromo-2-naphthoate
CAS:<p>Methyl 6-bromo-2-naphthoate is an eluting compound that binds with a hydroxyl group to the gamma-aminobutyric acid receptor. It has been shown to have high binding constants and the ability to bind to protein data. Methyl 6-bromo-2-naphthoate has been shown to inhibit the production of GABA in fetal bovine brain slices, which may be due to its ability to bind selectively with this receptor. This agent also inhibits cell proliferation and induces cell death in culture by interacting with proteins involved in cell cycle regulation.</p>Formula:C12H9BrO2Purity:Min. 95%Color and Shape:PowderMolecular weight:265.1 g/molMethyl 6-bromo-2-naphthoate
CAS:Formula:C12H9BrO2Purity:95%Color and Shape:White – Pale yellow powderMolecular weight:265.106











