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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)-

ethyl 3-amino-4-iodobenzoate

CCOC(=O)c1ccc(c(c1)N)I Request for Quotation
Chemical Name: ethyl 3-amino-4-iodobenzoate
CAS Number: 1261569-51-0
Product Number: AG000RV1(AGN-PC-0D3RC2)
Synonyms:
MDL No:
Molecular Formula: C9H10INO2
Molecular Weight: 291.0857

Identification/Properties

Computed Properties
Molecular Weight:
291.088g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
290.976g/mol
Monoisotopic Mass:
290.976g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
187
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


Ethyl 3-amino-4-iodobenzoate is a versatile compound widely utilized in chemical synthesis due to its unique reactivity and functional group diversity. This compound serves as a key building block in organic chemistry, particularly in the creation of various pharmaceuticals, agrochemicals, and advanced materials.Its precise structure allows for selective transformations, making it a valuable reagent in the creation of complex molecules through various chemical reactions. Ethyl 3-amino-4-iodobenzoate's amino and ester functionalities provide opportunities for further derivatization, enabling the synthesis of diverse compounds with specific properties and functions for various applications.In organic synthesis, this compound can participate in cross-coupling reactions, such as Suzuki coupling, Sonogashira coupling, and Buchwald-Hartwig amination, to form intricate molecular frameworks. Additionally, its iodine atom can act as a leaving group in substitution reactions, leading to the introduction of new functional groups or structural modifications.Overall, Ethyl 3-amino-4-iodobenzoate plays a crucial role in chemical synthesis by facilitating the construction of molecular scaffolds with tailored properties, making it an indispensable tool for researchers and chemists in the development of novel compounds for a wide range of industries.