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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Amino-5-chloro-4-iodophenol

Oc1cc(Cl)c(cc1N)I Request for Quotation
Chemical Name: 2-Amino-5-chloro-4-iodophenol
CAS Number: 1037298-24-0
Product Number: AG00975P(AGN-PC-0WAMDW)
Synonyms:
MDL No: MFCD27978469
Molecular Formula: C6H5ClINO
Molecular Weight: 269.4675

Identification/Properties

Computed Properties
Molecular Weight:
269.466g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
268.91g/mol
Monoisotopic Mass:
268.91g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
124
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


2-Amino-5-chloro-4-iodophenol, also known by its chemical formula C6H5ClINO, plays a crucial role in chemical synthesis as a versatile building block. This compound is utilized in the synthesis of various pharmaceuticals, dyes, and agrochemicals due to its unique chemical properties.One of the key applications of 2-Amino-5-chloro-4-iodophenol is its use as a precursor in the synthesis of biologically active molecules. By incorporating this compound into synthetic pathways, chemists can access a wide range of structurally diverse compounds that exhibit pharmacological activities. This versatility makes 2-Amino-5-chloro-4-iodophenol a valuable tool in the development of new drugs and therapeutic agents.Furthermore, the presence of both amino and halogen functional groups in this molecule allows for selective derivatization and modification, enabling chemists to tailor the properties of the final products. This flexibility is particularly advantageous in medicinal chemistry, where fine-tuning the structure of a compound can significantly impact its biological activity and pharmacokinetic profile.In addition to pharmaceutical applications, 2-Amino-5-chloro-4-iodophenol is also employed in the synthesis of dyes and pigments. Its ability to participate in various chemical reactions, such as aromatic substitution and coupling reactions, makes it a valuable building block for the production of colorful and high-performance dye molecules.Overall, the strategic placement of functional groups in 2-Amino-5-chloro-4-iodophenol lends itself well to diverse chemical transformations, making it a versatile and indispensable compound in modern chemical synthesis.