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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-Thiazoleacetonitrile, 4-methyl-

Cc1csc(n1)CC#N Request for Quotation
Chemical Name: 2-Thiazoleacetonitrile, 4-methyl-
CAS Number: 19785-39-8
Product Number: AG002B4B(AGN-PC-0JVOPQ)
Synonyms:
MDL No:
Molecular Formula: C6H6N2S
Molecular Weight: 138.1902

Identification/Properties

Computed Properties
Molecular Weight:
138.188g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
138.025g/mol
Monoisotopic Mass:
138.025g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
137
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Methylthiazol-2-yl)acetonitrile, also known as $name$, is a versatile chemical compound commonly used in organic synthesis for its valuable properties. This compound plays a crucial role in various chemical reactions due to its unique structure and reactivity. In chemical synthesis, 2-(4-Methylthiazol-2-yl)acetonitrile serves as a key building block for the production of pharmaceuticals, agrochemicals, and fine chemicals.One primary application of 2-(4-Methylthiazol-2-yl)acetonitrile is as a precursor in the synthesis of biologically active molecules. Its thiazole ring and acetonitrile group provide a useful platform for creating complex structures with specific biological activities. By incorporating this compound into a synthesis pathway, chemists can access diverse chemical structures that exhibit pharmacological or biological properties, making it a valuable tool in drug discovery and development.Furthermore, 2-(4-Methylthiazol-2-yl)acetonitrile can function as a nucleophilic reagent in various organic transformations. Its electron-rich thiazole moiety enables it to participate in nucleophilic substitution reactions, forming new carbon-carbon or carbon-heteroatom bonds. This reactivity expands the possibilities for creating novel molecules with desired properties, making it a versatile reagent in organic chemistry.Overall, the application of 2-(4-Methylthiazol-2-yl)acetonitrile in chemical synthesis demonstrates its significance as a key intermediate in the production of complex molecules with pharmaceutical, agricultural, or industrial relevance. Its versatile reactivity and structural features make it a valuable tool for synthetic chemists seeking to access diverse chemical space and develop new compounds with potential applications in various fields.