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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)-

4-Thiazolecarboxylic acid, 2-amino-

Nc1nc(cs1)C(=O)O Request for Quotation
Chemical Name: 4-Thiazolecarboxylic acid, 2-amino-
CAS Number: 40283-41-8
Product Number: AG00BXZY(AGN-PC-0K63TE)
Synonyms:
MDL No:
Molecular Formula: C4H4N2O2S
Molecular Weight: 144.1518

Identification/Properties

Properties
MP:
171-181 °C(lit.);
BP:
415°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
144.148g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
143.999g/mol
Monoisotopic Mass:
143.999g/mol
Topological Polar Surface Area:
104A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
130
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:
H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Aminothiazole-4-carboxylic acid is a versatile building block in chemical synthesis, commonly utilized in the production of various pharmaceuticals, agrochemicals, and materials. With its unique structure and reactive properties, this compound plays a crucial role in the creation of complex organic molecules through a variety of synthetic routes. In particular, 2-Aminothiazole-4-carboxylic acid serves as a key intermediate in the synthesis of bioactive compounds and drug molecules due to its functional groups that enable further derivatization and modification. Its application in peptide coupling reactions, heterocycle formation, and transition metal catalysis showcases its significance in the field of synthetic chemistry.