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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-amino-5-methyl-, methyl ester

Cc1sc(nc1CC(=O)OC)N Request for Quotation
Chemical Name: 4-Thiazoleacetic acid, 2-amino-5-methyl-, methyl ester
CAS Number: 259654-73-4
Product Number: AG002R7S(AGN-PC-0KKPMG)
Synonyms:
MDL No: MFCD00662517
Molecular Formula: C7H10N2O2S
Molecular Weight: 186.2315

Identification/Properties

Properties
BP:
324.2±27.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
186.229g/mol
XLogP3:
0.8
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:
H302-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-(2-amino-5-methylthiazol-4-yl)acetate, commonly referred to as $name$, serves as a valuable chemical building block in organic synthesis. This compound is widely employed as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its versatile reactivity and functional group compatibility. In chemical synthesis, $name$ is utilized as a precursor for the synthesis of heterocyclic compounds, which are essential in the development of bioactive molecules with diverse applications. Its unique structure and reactivity make it a valuable tool in the construction of complex molecular frameworks, enabling chemists to access new compounds with potential therapeutic or industrial significance. By incorporating $name$ into synthetic pathways, chemists can efficiently access a wide range of target molecules with tailored properties and functionalities, highlighting its pivotal role in modern organic synthesis practices.