CAS 20717-80-0: 3-Bromo-2-naphthalenecarboxylic acid
Formula:C11H7BrO2
InChI:InChI=1S/C11H7BrO2/c12-10-6-8-4-2-1-3-7(8)5-9(10)11(13)14/h1-6H,(H,13,14)
InChI key:InChIKey=KJEICVAXCBDOSH-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=CC2=C(C=C1Br)C=CC=C2
Synonyms:- 2-Bromo-3-naphthalenecarboxylic acid
- 2-Naphthoic acid, 3-bromo-
- 3-Bromo-2-naphthalenecarboxylic acid
- 3-Bromo-2-naphthoic acid
- 3-Bromonaphthalene-2-Carboxylic Acid
- 2-Naphthalenecarboxylic acid, 3-bromo-
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Found 5 products.
3-Bromo-2-naphthoic acid
CAS:3-Bromo-2-naphthoic acid is a hydroxy derivative of 2-naphthol. It has been shown to bind to guanine in DNA and form covalent adducts, leading to the disruption of DNA synthesis and replication. 3-Bromo-2-naphthoic acid also inhibits the activity of DNA polymerase, leading to an accumulation of single stranded DNA molecules. This drug can cause exocyclic alkylation of deoxyguanosine residues, leading to significant cytotoxic effects on tumor cells. 3-Bromo-2-naphthoic acid has significant cytotoxic activity against a wide range of cancer cell lines at low concentrations.Formula:C11H7BrO2Purity:Min. 95%Molecular weight:251.08 g/molRef: 3D-VAA71780
Discontinued product2-Naphthalenecarboxylic acid, 3-bromo-
CAS:Formula:C11H7BrO2Purity:97%Color and Shape:SolidMolecular weight:251.07613-Bromo-2-naphthoic Acid
CAS:Controlled ProductApplications 3-Bromo-2-naphthoic Acid is used as a reagent for prepartion of isochromanones. References Wen, Z.K., et al.: Advanced Synthesis and Catalysis, 361,963 (2019)Formula:C11H7BrO2Color and Shape:NeatMolecular weight:251.0763-Bromonaphthalene-2-carboxylic acid
CAS:3-Bromonaphthalene-2-carboxylic acidPurity:95%Molecular weight:251.08g/mol
