CAS 95-85-2
:2-Amino-4-chlorophenol
Description:
2-Amino-4-chlorophenol, with the CAS number 95-85-2, is an organic compound characterized by the presence of an amino group (-NH2) and a chlorophenol structure. It appears as a solid, typically in a crystalline form, and is known for its light yellow to brown color. This compound is soluble in water and organic solvents, which makes it useful in various applications. It is primarily utilized in the dye industry, particularly for the synthesis of azo dyes, and also serves as an intermediate in the production of pharmaceuticals and agrochemicals. The presence of the amino and chloro groups contributes to its reactivity, allowing it to participate in electrophilic substitution reactions. Additionally, 2-amino-4-chlorophenol exhibits certain biological activities, which may include antimicrobial properties. However, safety precautions are necessary when handling this compound, as it may pose health risks, including skin and respiratory irritation. Proper storage and disposal methods should be followed to mitigate environmental impact.
Formula:C6H6ClNO
InChI:InChI=1S/C6H6ClNO/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,8H2
InChI key:InChIKey=SWFNPENEBHAHEB-UHFFFAOYSA-N
SMILES:NC1=C(O)C=CC(Cl)=C1
Synonyms:- 1-Amino-2-hydroxy-5-chlorobenzene
- 1-Hydroxy-2-amino-4-chlorobenzene
- 2-Amino-4-Clorofenol
- 2-Amino-4-chlorophenol
- 2-Amino-4-chlorphenol
- 2-Hydroxy-5-chloroaniline
- 4-Chloro-o-aminophenol
- 4-chloro-2-Aminophenol
- Aminochlorophenol
- Fouramine PY
- Nsc 247814
- Phenol, 2-amino-4-chloro-
- o-Amino-p-chlorophenol
- p-Chloro-o-Aminophenol
- C.I. Oxidation Base 18
- C.I. Oxidation Base 18
- See more synonyms
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Found 10 products.
Chlorzoxazone Related Compound A (2-Amino-4-chlorophenol)
CAS:Amino-naphthols and other amino-phenols, their ethers aFormula:C6H6ClNOColor and Shape:Brown Crystalline PowderMolecular weight:143.013792-Amino-4-chlorophenol
CAS:Formula:C6H6ClNOPurity:≥ 97.5%Color and Shape:Off-white to grey, beige or pale yellow powder or crystalsMolecular weight:143.57Chlorzoxazone USP Related Compound A
CAS:Controlled ProductFormula:C6H6ClNOColor and Shape:NeatMolecular weight:143.572-Amino-4-chlorophenol
CAS:Controlled ProductFormula:C6H6ClNOColor and Shape:NeatMolecular weight:143.572-Amino-4-chlorophenol
CAS:Formula:C6H6ClNOPurity:>98.0%(GC)(T)Color and Shape:White to Gray to Brown powder to crystalMolecular weight:143.57Chlorzoxazone USP Related Compound A (2-Amino-4-Chlorophenol)
CAS:Formula:C6H6ClNOMolecular weight:143.572-Amino-4-chlorophenol
CAS:<p>Applications 2-Amino-4-chlorophenol is a widely used reagent in the synthesis of various drugs, dyes and pesticides. A reagent in the synthesis of aggrecanase-2 inhibitors based on acylthiosemicarbazide zinc-binding, used in the treatment of osteoarthritis.<br>References Arora, P. et al.: Microb. Cell Fact., 11, 150 (2012); Maingot, L. et al.: Eur. J. Med. CHem., 69, 244 (2013);<br></p>Formula:C6H6ClNOColor and Shape:BeigeMolecular weight:143.574-Chloro-2-aminophenol
CAS:<p>4-Chloro-2-aminophenol is a chemical compound that can be found in nature or synthesized. It has antibacterial properties and is used as an antimicrobial agent. 4-Chloro-2-aminophenol inhibits the growth of bacteria by inhibiting nitrogenase enzyme activity, which is required for the production of amino acids and nucleic acids. This compound also induces cytotoxicity and significant cell death in colorectal adenocarcinoma cells. 4-Chloro-2-aminophenol is a weak acid that reacts with hydrochloric acid to form a diazonium salt, which reacts with benzene to form an intramolecular hydrogen bond. The final product of this reaction is a solid phase microextraction (SPME) sorbent that can be used to extract analytes from liquid samples.</p>Formula:C6H6ClNOPurity:Min. 95%Molecular weight:143.57 g/mol
