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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)-

5-Thiazolecarboxamide, 2-amino-N-(2-chloro-6-methylphenyl)-

Nc1ncc(s1)C(=O)Nc1c(C)cccc1Cl Request for Quotation
Chemical Name: 5-Thiazolecarboxamide, 2-amino-N-(2-chloro-6-methylphenyl)-
CAS Number: 302964-24-5
Product Number: AG002ZJG(AGN-PC-03HLHP)
Synonyms:
MDL No:
Molecular Formula: C11H10ClN3OS
Molecular Weight: 267.7346

Identification/Properties

Properties
MP:
208.0 to 212.0 °C
BP:
362°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
267.731g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
267.023g/mol
Monoisotopic Mass:
267.023g/mol
Topological Polar Surface Area:
96.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
292
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-N-(2-chloro-6-methylphenyl)thiazole-5-carboxamide is a versatile compound widely used in chemical synthesis as a building block for the construction of various biologically active molecules. Due to its unique structure and reactivity, this compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.In organic synthesis, 2-Amino-N-(2-chloro-6-methylphenyl)thiazole-5-carboxamide can undergo a variety of transformations such as nucleophilic substitution, cyclization reactions, and cross-coupling reactions to introduce different functional groups and create complex molecular architectures. This compound's functional groups enable selective modifications, facilitating the design and preparation of novel compounds with desired properties.Furthermore, the presence of the thiazole ring in 2-Amino-N-(2-chloro-6-methylphenyl)thiazole-5-carboxamide imparts unique characteristics to the molecules derived from it, making them potentially useful in various applications such as medicinal chemistry, material science, and chemical biology. The compound's structural features offer opportunities for molecular diversity and the exploration of structure-activity relationships in drug discovery and development.Overall, the versatility and reactivity of 2-Amino-N-(2-chloro-6-methylphenyl)thiazole-5-carboxamide make it an indispensable tool for chemists engaged in the synthesis of diverse chemical compounds with potential applications in various fields.