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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-bromo-5-phenyl-1,3-thiazole

Brc1ncc(s1)c1ccccc1 Request for Quotation
Chemical Name: 2-bromo-5-phenyl-1,3-thiazole
CAS Number: 133311-51-0
Product Number: AG0014LC(AGN-PC-0N9K8S)
Synonyms:
MDL No:
Molecular Formula: C9H6BrNS
Molecular Weight: 240.1196

Identification/Properties

Computed Properties
Molecular Weight:
240.118g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
238.94g/mol
Monoisotopic Mass:
238.94g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
148
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-H315-H319-H335
Precautionary Statements:
P260-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-5-phenylthiazole is a versatile compound widely used in chemical synthesis for its unique properties and applications. This organic heterocyclic compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-Bromo-5-phenylthiazole serves as a valuable building block for the construction of complex molecules due to its reactive bromine functional group and aromatic phenylthiazole core. It can undergo various chemical reactions, such as nucleophilic substitution and coupling reactions, to introduce additional functional groups and modify its structure.One of the key applications of 2-Bromo-5-phenylthiazole is in the synthesis of bioactive compounds, including pharmaceutical drugs and agrochemicals. By incorporating this compound into the molecular structure, researchers can fine-tune the properties of the final product, such as enhancing biological activity or improving chemical stability.Furthermore, 2-Bromo-5-phenylthiazole can also be used in material science for the development of novel organic semiconductors, fluorescent dyes, and other functional materials. Its unique chemical structure and reactivity make it a valuable tool for creating advanced materials with tailored properties for various applications.Overall, the versatility and reactivity of 2-Bromo-5-phenylthiazole make it a valuable compound in chemical synthesis, enabling the creation of diverse molecules with applications in pharmaceuticals, agrochemicals, and materials science.