6-Methoxy-2-naphthoic acid - CAS 2471-70-7
Catalog: |
BB018596 |
Product Name: |
6-Methoxy-2-naphthoic acid |
CAS: |
2471-70-7 |
Synonyms: |
6-methoxynaphthalene-2-carboxylic acid |
IUPAC Name: | 6-methoxynaphthalene-2-carboxylic acid |
Description: | A metabolite of Naproxen, which is a non-selective COX inhibitor. |
Molecular Weight: | 202.21 |
Molecular Formula: | C12H10O3 |
Canonical SMILES: | COC1=CC2=C(C=C1)C=C(C=C2)C(=O)O |
InChI: | InChI=1S/C12H10O3/c1-15-11-5-4-8-6-10(12(13)14)3-2-9(8)7-11/h2-7H,1H3,(H,13,14) |
InChI Key: | YZBILXXOZFORFE-UHFFFAOYSA-N |
Boiling Point: | 371.1 ℃ at 760 mmHg |
Purity: | 97 % |
Density: | 1.263 g/cm3 |
Appearance: | White to off-white solid |
MDL: | MFCD00092750 |
LogP: | 2.54660 |
GHS Hazard Statement: | H315 (97.83%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112679367-A | Naphthol derivative compound with analgesic activity and preparation method thereof | 20201229 |
CN-111254457-A | Electrochemical synthesis method of aromatic carboxylic acid and alkyl carboxylic acid | 20200331 |
CN-111254457-B | Electrochemical synthesis method of aromatic carboxylic acid and alkyl carboxylic acid | 20200331 |
CN-111413849-A | Photosensitive composition, preparation method thereof, pattern forming method and application | 20200115 |
WO-2021057813-A1 | Sulfimide photo-acid generator, photosensitive resin composition, patterning method, use of photosensitive resin composition | 20190925 |
PMID | Publication Date | Title | Journal |
22424148 | 20120412 | Fragment-based design of symmetrical bis-benzimidazoles as selective inhibitors of the trimethoprim-resistant, type II R67 dihydrofolate reductase | Journal of medicinal chemistry |
16730993 | 20060901 | Design, synthesis and evaluation of naphthalene-2-carboxamides as reversal agents in MDR cancer | Bioorganic & medicinal chemistry |
16041838 | 20050801 | Synthesis of some new 2-(6-methoxy-2-naphthyl)- 5-aryl-1,3,4-oxadiazoles as possible non-steroidal anti-inflammatory and analgesic agents | Archiv der Pharmazie |
1407 | 19751224 | [Template chromatography on immobilized oligonucleotides. Synthesis and application of oligodeoxyadenosine-5'-phosphate--DEAE-cellulose (author's transl)] | Journal of chromatography |
Complexity: | 239 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 202.062994177 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 202.062994177 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 46.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.3 |
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