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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)-

Benzoic acid, 2-amino-6-iodo-

OC(=O)c1c(N)cccc1I Request for Quotation
Chemical Name: Benzoic acid, 2-amino-6-iodo-
CAS Number: 20776-52-7
Product Number: AG002J9J(AGN-PC-0NK5XW)
Synonyms:
MDL No:
Molecular Formula: C7H6INO2
Molecular Weight: 263.0325

Identification/Properties

Computed Properties
Molecular Weight:
263.034g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
262.944g/mol
Monoisotopic Mass:
262.944g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
163
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-6-iodobenzoic acid is a valuable building block in chemical synthesis due to its versatile reactivity and unique properties. This compound is commonly used as a starting material in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials. Its ability to undergo nucleophilic substitution reactions makes it a key intermediate in the preparation of complex organic molecules. Additionally, the presence of both amino and carboxylic acid functionalities in 2-Amino-6-iodobenzoic acid allows for further derivatization, enabling the introduction of diverse functional groups for fine-tuning the properties of the final product. Furthermore, its specific structural features make it a useful precursor in the synthesis of biologically active compounds and novel chemical entities with potential applications in drug discovery and materials science.