CAS 6358-07-2: 2-Amino-4-chloro-5-nitrophenol
Formula:C6H5ClN2O3
InChI:InChI=1S/C6H5ClN2O3/c7-3-1-4(8)6(10)2-5(3)9(11)12/h1-2,10H,8H2
InChI key:InChIKey=ZARYBZGMUVAJMK-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(Cl)C=C(N)C(O)=C1
Synonyms:- 2-Amino-5-Nitro-4-Chlorophenol
- 4-Chloro-5-nitro-2-aminophenol
- NSC 7537
- Phenol, 2-amino-4-chloro-5-nitro-
- 2-Amino-4-chloro-5-nitrophenol
- 2-Amino-4-chloro-5-nitrophenol
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Found 5 products.
Phenol, 2-amino-4-chloro-5-nitro-
CAS:Formula:C6H5ClN2O3Purity:98%Color and Shape:SolidMolecular weight:188.56852-Amino-4-chloro-5-nitrophenol
CAS:Purity:95.0%Color and Shape:Solid, Yellow to yellow red powderMolecular weight:188.570007324218752-Amino-4-chloro-5-nitrophenol
CAS:2-Amino-4-chloro-5-nitrophenolColor and Shape:SolidMolecular weight:188.57g/mol2-Amino-4-chloro-5-nitrophenol
CAS:2-Amino-4-chloro-5-nitrophenol is a chemical that is synthesized in the laboratory and can be used as an acetylating agent. Acetylation is a chemical reaction that adds an acetyl group to a molecule. 2-Amino-4-chloro-5-nitrophenol is a conjugate of chloroacetaldehyde with 2,4,5,6 tetranitrobenzene and has potent cytotoxicity against MDA MB231 breast cancer cells. The anticancer activity of 2 amino 4 chloro 5 nitrophenol has been demonstrated in vitro by inhibiting the enzyme activity of glutathione S transferase. This agent also inhibits the growth of cancer cells by binding to chloride ions and forming a complex with palladium. 2 amino 4 chloro 5 nitrophenol can react with hydroxyl groups on proteins or DNA bases to form adducts which are moreFormula:C6H5ClN2O3Purity:Min. 95%Molecular weight:188.57 g/molRef: 3D-FA36755
Discontinued product2-Amino-4-chloro-5-nitrophenol
CAS:Formula:C6H5ClN2O3Purity:>98.0%(T)(HPLC)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:188.57
