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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-5-ethyl-, methyl ester

COC(=O)c1nc(sc1CC)N Request for Quotation
Chemical Name: 4-Thiazolecarboxylic acid, 2-amino-5-ethyl-, methyl ester
CAS Number: 28942-54-3
Product Number: AG002X54(AGN-PC-0JVOX7)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O2S
Molecular Weight: 186.2315

Identification/Properties

Properties
MP:
120-122°C
BP:
341.9°C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
186.229g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
186.046g/mol
Monoisotopic Mass:
186.046g/mol
Topological Polar Surface Area:
93.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
177
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:
H317
Precautionary Statements:
P261-P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-amino-5-ethylthiazole-4-carboxylate is a versatile compound commonly used in chemical synthesis due to its unique properties. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its presence in a synthetic pathway can enable the introduction of the thiazole ring system, which imparts specific chemical and biological activities to the final product. Methyl 2-amino-5-ethylthiazole-4-carboxylate is particularly valued for its ability to enhance the functionality and diversity of organic molecules, making it a valuable tool for chemists in the development of novel compounds with desired properties. Its strategic incorporation in chemical synthesis can lead to the creation of new molecules with potential applications in drug discovery, material science, and other fields that require custom-designed molecules.