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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)-

2-Thiazolamine, 5-bromo-4-(trifluoromethyl)-

Nc1sc(c(n1)C(F)(F)F)Br Request for Quotation
Chemical Name: 2-Thiazolamine, 5-bromo-4-(trifluoromethyl)-
CAS Number: 136411-21-7
Product Number: AG007MJN(AGN-PC-0NKQ9B)
Synonyms:
MDL No:
Molecular Formula: C4H2BrF3N2S
Molecular Weight: 247.0363

Identification/Properties

Computed Properties
Molecular Weight:
247.033g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
245.907g/mol
Monoisotopic Mass:
245.907g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-4-(trifluoromethyl)thiazol-2-amine is a versatile chemical compound that finds wide application in chemical synthesis. It serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties.In chemical synthesis, this compound is often utilized as a key intermediate in the development of new drug candidates. Its functional groups enable efficient derivatization, allowing for the modification of its chemical structure to generate diverse analogs for biological testing and optimization of desired properties. Additionally, its incorporation into heterocyclic scaffolds enhances the bioactivity and potency of the final molecules.Furthermore, 5-Bromo-4-(trifluoromethyl)thiazol-2-amine plays a significant role in the preparation of fluorinated compounds, which are of particular interest in medicinal chemistry and material science. The trifluoromethyl group imparts desirable physicochemical characteristics to the target molecules, such as increased lipophilicity and metabolic stability, leading to enhanced drug-like properties.Overall, the strategic use of 5-Bromo-4-(trifluoromethyl)thiazol-2-amine in chemical synthesis underscores its importance as a valuable tool for the construction of complex molecules with potential applications across various scientific disciplines.