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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)-

5-(Hydroxymethyl)-2-iodophenol

OCc1ccc(c(c1)O)I Request for Quotation
Chemical Name: 5-(Hydroxymethyl)-2-iodophenol
CAS Number: 773869-57-1
Product Number: AG005BKR(AGN-PC-0WAMMO)
Synonyms:
MDL No: MFCD06202863
Molecular Formula: C7H7IO2
Molecular Weight: 250.0337

Identification/Properties

Properties
MP:
148 °C
BP:
273.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
250.035g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
249.949g/mol
Monoisotopic Mass:
249.949g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
108
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(Hydroxymethyl)-2-iodophenol, an important chemical compound, plays a crucial role in various chemical synthesis processes. This versatile compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals. With its unique structure, 5-(Hydroxymethyl)-2-iodophenol offers a valuable starting point for the synthesis of complex organic molecules. Its hydroxyl group enables it to participate in a range of reactions, including nucleophilic substitution, oxidation, and coupling reactions. Through its involvement in chemical synthesis, 5-(Hydroxymethyl)-2-iodophenol contributes to the development of new materials and compounds with diverse applications in industries such as medicine, agriculture, and materials science.