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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-chloro-1,3-thiazole-4-carbonitrile

Clc1nc(cs1)C#N Request for Quotation
Chemical Name: 2-chloro-1,3-thiazole-4-carbonitrile
CAS Number: 944124-72-5
Product Number: AG005XIE(AGN-PC-07AUI9)
Synonyms:
MDL No:
Molecular Formula: C4HClN2S
Molecular Weight: 144.5821

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
144.576g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
143.955g/mol
Monoisotopic Mass:
143.955g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
129
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:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chlorothiazole-4-carbonitrile is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 2-Chlorothiazole-4-carbonitrile can act as a key intermediate for the synthesis of thiazole-based compounds, which are essential in drug development and organic synthesis. Its presence as a nitrile group allows for further functionalization, enabling the introduction of various substituents to tailor the molecule's properties for specific applications.Additionally, the chlorine atom on the thiazole ring can undergo substitution reactions to create new derivatives with different physicochemical characteristics. This versatility makes 2-Chlorothiazole-4-carbonitrile a valuable tool for organic chemists seeking to modify and design novel compounds with potential biological activities or industrial applications.