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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)-

2-lodo-3-thiophencarboxylicacid

OC(=O)c1ccsc1I Request for Quotation
Chemical Name: 2-lodo-3-thiophencarboxylicacid
CAS Number: 18895-00-6
Product Number: AG002HLE(AGN-PC-0WA6UM)
Synonyms:
MDL No:
Molecular Formula: C5H3IO2S
Molecular Weight: 254.0456

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
254.041g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
253.89g/mol
Monoisotopic Mass:
253.89g/mol
Topological Polar Surface Area:
65.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
128
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-Iodothiophene-3-carboxylic acid is a versatile building block in chemical synthesis due to its unique structural properties and reactivity. It is commonly used in the preparation of various organic compounds, especially in the pharmaceutical and agrochemical industries.This compound can serve as a valuable precursor in the synthesis of heterocyclic compounds, such as thiophenes, which are important scaffolds in medicinal chemistry. By incorporating 2-Iodothiophene-3-carboxylic acid into a synthetic route, chemists can access a wide range of derivatives with tailored properties and functionalities.Additionally, the presence of the iodo group offers opportunities for further functionalization through cross-coupling reactions, allowing for the introduction of different substituents or complex molecular motifs. This versatility makes 2-Iodothiophene-3-carboxylic acid a valuable tool for the construction of diverse molecular architectures in organic synthesis.Overall, the strategic use of 2-Iodothiophene-3-carboxylic acid in chemical synthesis enables the efficient and selective formation of complex organic molecules with potential applications in drug discovery, materials science, and other fields.