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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)-

Phenol, 2-amino-5-iodo-

Ic1ccc(c(c1)O)N Request for Quotation
Chemical Name: Phenol, 2-amino-5-iodo-
CAS Number: 99968-80-6
Product Number: AG003VL1(AGN-PC-02LCGI)
Synonyms:
MDL No:
Molecular Formula: C6H6INO
Molecular Weight: 235.0224

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
235.024g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
234.949g/mol
Monoisotopic Mass:
234.949g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
9
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-5-iodophenol, also known as 2-AIOP, is a versatile compound extensively utilized in chemical synthesis processes. This compound serves as a crucial building block in the construction of various organic molecules and pharmaceutical intermediates due to its unique chemical properties. In chemical synthesis, 2-Amino-5-iodophenol plays a vital role as a key starting material for the production of a wide range of compounds. Its amino and iodine functional groups allow for diverse functionalization reactions, enabling the synthesis of complex structures with specific applications in the pharmaceutical, agrochemical, and materials industries. One notable application of 2-Amino-5-iodophenol is its use in the synthesis of biologically active molecules and pharmaceuticals. By reacting with other reagents or undergoing specific chemical transformations, this compound can be incorporated into drug candidates or intermediates with potential therapeutic properties. Its ability to form stable bonds and participate in various organic reactions makes it a valuable tool for medicinal chemistry research and development.Additionally, 2-Amino-5-iodophenol finds utility in the preparation of dyes, pigments, and specialty chemicals. Through controlled chemical modifications, this compound can be tailored to exhibit specific color properties or functional characteristics, making it suitable for various industrial applications. Its versatility and reactivity make it a sought-after component in the synthesis of diverse chemical products with distinct properties and functionalities.