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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)-

4-methyl-2-(pyrrolidin-3-yl)-1,3-thiazole

Cc1csc(n1)C1CNCC1 Request for Quotation
Chemical Name: 4-methyl-2-(pyrrolidin-3-yl)-1,3-thiazole
CAS Number: 1257521-56-4
Product Number: AG01BTKV(AG01BTKV)
Synonyms:
MDL No:
Molecular Formula: C8H12N2S
Molecular Weight: 168.2593

Identification/Properties

Computed Properties
Molecular Weight:
168.258g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
168.072g/mol
Monoisotopic Mass:
168.072g/mol
Topological Polar Surface Area:
53.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methyl-2-(pyrrolidin-3-yl)-1,3-thiazole is a versatile compound commonly utilized in chemical synthesis due to its unique chemical properties and functional groups. This compound can serve as a valuable building block in the creation of various organic molecules and pharmaceuticals. In chemical synthesis, 4-Methyl-2-(pyrrolidin-3-yl)-1,3-thiazole can act as a key intermediate in the production of complex heterocyclic compounds. Its pyrrolidine and thiazole rings provide opportunities for further functionalization through various synthetic transformations, allowing for the introduction of different chemical groups and modifications. Additionally, the presence of the methyl group offers the potential for stereochemical control in the synthesis of chiral molecules. The diverse applications of 4-Methyl-2-(pyrrolidin-3-yl)-1,3-thiazole in chemical synthesis make it a valuable tool for creating novel compounds with desired properties.