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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-Thiophenecarboxylic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-

O=C(Nc1ccsc1C(=O)O)OC(C)(C)C Request for Quotation
Chemical Name: 2-Thiophenecarboxylic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-
CAS Number: 101537-64-8
Product Number: AG0004Q3(AGN-PC-0KKLAE)
Synonyms:
MDL No:
Molecular Formula: C10H13NO4S
Molecular Weight: 243.2795

Identification/Properties

Computed Properties
Molecular Weight:
243.277g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
243.057g/mol
Monoisotopic Mass:
243.057g/mol
Topological Polar Surface Area:
104A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
287
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(N-Boc-amino)thiophene-2-carboxylic acid, a versatile building block in chemical synthesis, is utilized primarily for its ability to introduce an N-Boc-protected amino group onto the thiophene ring. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. The N-Boc protecting group ensures selective reactivity of the amino group, allowing for further functionalization reactions without affecting other reactive sites. Furthermore, the presence of the thiophene ring confers unique electronic properties to the molecule, making it valuable in the development of diverse organic compounds with desired properties. In medicinal chemistry, 3-(N-Boc-amino)thiophene-2-carboxylic acid is especially valuable for the construction of bioactive molecules, as the presence of both the amino group and thiophene ring can enhance the pharmacological properties of the final products. Its strategic placement within a molecular scaffold can greatly influence the compound's biological activity, aiding in the design and optimization of potential drug candidates. In summary, the incorporation of 3-(N-Boc-amino)thiophene-2-carboxylic acid in chemical synthesis offers a powerful means to access structurally diverse and biologically relevant molecules with tailored functionalities.