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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-iodo-4,5-dimethoxy-, methyl ester

COC(=O)c1cc(OC)c(cc1I)OC Request for Quotation
Chemical Name: Benzoic acid, 2-iodo-4,5-dimethoxy-, methyl ester
CAS Number: 173043-61-3
Product Number: AG003RO7(AGN-PC-00FKWM)
Synonyms:
MDL No:
Molecular Formula: C10H11IO4
Molecular Weight: 322.0964

Identification/Properties

Properties
MP:
105-107°C
BP:
352.8±42.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
322.098g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
321.97g/mol
Monoisotopic Mass:
321.97g/mol
Topological Polar Surface Area:
44.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
222
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


Methyl 2-iodo-4,5-dimethoxybenzoate, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as an important building block in the creation of various organic molecules due to its unique structural properties and reactivity. In chemical synthesis, $name$ is commonly employed as a key intermediate in the preparation of complex pharmaceuticals, agrochemicals, and functional materials. Its specific application lies in its ability to undergo various chemical transformations, such as substitution reactions, coupling reactions, and rearrangements, leading to the formation of diverse organic products with tailored functionalities. By incorporating $name$ into synthetic pathways, chemists can efficiently access a wide range of structurally intricate compounds, making it a valuable tool in modern organic synthesis.