Phenol, 4-amino-3-chloro-, hydrochloride


Chemical Name: Phenol, 4-amino-3-chloro-, hydrochloride
CAS Number: 52671-64-4
Product Number: AG003KPD(AGN-PC-0NJJYP)
Synonyms:
MDL No: MFCD00143110
Molecular Formula: C6H7Cl2NO
Molecular Weight: 180.0319

Identification/Properties


Properties
MP:
255 °C(dec.)(lit.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
180.028g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
178.99g/mol
Monoisotopic Mass:
178.99g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
99.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Amino-3-chlorophenol hydrochloride is a versatile chemical compound commonly used in the field of chemical synthesis. Due to its unique properties, this substance plays a crucial role in various chemical reactions and processes.One of the key applications of 4-Amino-3-chlorophenol hydrochloride in chemical synthesis is its use as a building block in the production of dyes and pigments. This compound serves as a precursor in the synthesis of azo dyes, which are widely utilized in the textile industry for coloring fabrics. Additionally, it is involved in the formation of various colorants used in printing inks and paints.Furthermore, 4-Amino-3-chlorophenol hydrochloride is commonly employed in the pharmaceutical industry for the synthesis of biologically active compounds. It serves as a starting material for the production of various pharmaceutical agents, including antihistamines, anti-inflammatory drugs, and antibacterial medications. The compound's chemical structure allows for the modification and functionalization necessary to create new therapeutic compounds with specific bioactivities.In addition to its applications in dye and pharmaceutical synthesis, 4-Amino-3-chlorophenol hydrochloride is also utilized in the creation of specialty chemicals and intermediates. Its reactivity and functional groups make it a valuable component in the preparation of complex organic molecules, enabling the development of new materials, fine chemicals, and advanced technologies.Overall, 4-Amino-3-chlorophenol hydrochloride's role in chemical synthesis extends across diverse industries, highlighting its significance as a versatile building block for the production of a wide range of valuable products.