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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, 4-(4-bromophenyl)-

Brc1ccc(cc1)c1csc(n1)N Request for Quotation
Chemical Name: 2-Thiazolamine, 4-(4-bromophenyl)-
CAS Number: 2103-94-8
Product Number: AG002KOM(AGN-PC-0JTXCK)
Synonyms:
MDL No:
Molecular Formula: C9H7BrN2S
Molecular Weight: 255.1343

Identification/Properties

Computed Properties
Molecular Weight:
255.133g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
253.951g/mol
Monoisotopic Mass:
253.951g/mol
Topological Polar Surface Area:
67.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
171
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-4-(4-bromophenyl)thiazole is a versatile compound commonly utilized in chemical synthesis processes. Its unique structure and functional groups make it a valuable building block for the creation of various organic molecules. In organic chemistry, this compound is often employed as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other complex organic compounds. Its presence enables the introduction of specific functional groups or substituents that are crucial for fine-tuning the properties and activities of the final product. Additionally, the reactivity of 2-Amino-4-(4-bromophenyl)thiazole allows chemists to carry out diverse chemical transformations, making it a valuable tool in the arsenal of synthetic chemists. Whether used as a nucleophilic reagent, a catalyst precursor, or a key structural component, this compound plays a pivotal role in advancing the field of chemical synthesis.