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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-Thiazoleacetic acid, 2-methyl-, ethyl ester

CCOC(=O)Cc1csc(n1)C Request for Quotation
Chemical Name: 4-Thiazoleacetic acid, 2-methyl-, ethyl ester
CAS Number: 37128-24-8
Product Number: AG00C8Q7(AGN-PC-0JX2NY)
Synonyms:
MDL No:
Molecular Formula: C8H11NO2S
Molecular Weight: 185.2434

Identification/Properties

Properties
BP:
258.9°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
185.241g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
185.051g/mol
Monoisotopic Mass:
185.051g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
163
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:
H302
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Utilizing Ethyl 2-(2-methyl-1,3-thiazol-4-yl)-acetate in chemical synthesis offers a versatile approach for incorporating the thiazole moiety into various organic compounds. This compound serves as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and materials with diverse functionalities. Its unique structure provides opportunities for the design and creation of novel chemical entities with potential biological activities or tailored properties. By harnessing the reactivity of Ethyl 2-(2-methyl-1,3-thiazol-4-yl)-acetate, chemists can engage in elaborate transformations to access a wide array of structurally intricate molecules, paving the way for advancements in medicinal chemistry, materials science, and beyond.