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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)-

Thiazole, 2-chloro-4-phenyl-

Clc1scc(n1)c1ccccc1 Request for Quotation
Chemical Name: Thiazole, 2-chloro-4-phenyl-
CAS Number: 1826-23-9
Product Number: AG0023ZV(AGN-PC-0KKOLF)
Synonyms:
MDL No:
Molecular Formula: C9H6ClNS
Molecular Weight: 195.6686

Identification/Properties

Properties
MP:
54-58 °C
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
195.664g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
194.991g/mol
Monoisotopic Mass:
194.991g/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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H318-H335
Precautionary Statements:
P261-P280-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-4-phenylthiazole is a valuable building block in chemical synthesis due to its versatile reactivity and unique structural features. This compound is commonly used as a key intermediate in the production of various pharmaceuticals, agrochemicals, and materials.In organic chemistry, 2-Chloro-4-phenylthiazole serves as a useful starting material for the synthesis of diverse heterocyclic compounds. Its thiazole ring system provides a strong foundation for the creation of novel molecules with potentially beneficial properties. Through carefully designed chemical transformations, researchers can functionalize the chlorine atom and the phenyl group to introduce specific functionalities or structural motifs into the target molecules.Additionally, 2-Chloro-4-phenylthiazole can participate in various metal-catalyzed reactions, such as cross-coupling and cycloaddition reactions, to construct more complex molecular architectures. By utilizing the reactivity of the thiazole ring, chemists can access structurally diverse compounds with tailored properties for desired applications.Overall, the strategic incorporation of 2-Chloro-4-phenylthiazole in chemical synthesis enables the efficient construction of molecular libraries and the discovery of new compounds with potential biological or material-related activities. Its versatility and reactivity make it a valuable tool for organic chemists seeking to develop innovative molecules with specific functionalities and properties.