1. Home
  2. Pyrimidine, 4,5-dichloro-2-(methylthio)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Pyrimidine, 4,5-dichloro-2-(methylthio)-

CSc1ncc(c(n1)Cl)Cl Request for Quotation
Chemical Name: Pyrimidine, 4,5-dichloro-2-(methylthio)-
CAS Number: 99469-85-9
Product Number: AG0039FZ(AGN-PC-000W9W)
Synonyms:
MDL No:
Molecular Formula: C5H4Cl2N2S
Molecular Weight: 195.0697

Identification/Properties

Computed Properties
Molecular Weight:
195.061g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
193.947g/mol
Monoisotopic Mass:
193.947g/mol
Topological Polar Surface Area:
51.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
114
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4,5-Dichloro-2-(methylthio)pyrimidine is a versatile compound widely used in chemical synthesis as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and reactivity, this compound serves as an important intermediate in the synthesis of complex organic molecules. In particular, it is commonly employed in the preparation of heterocyclic compounds and bioactive molecules through different chemical reactions such as nucleophilic substitutions, cross-coupling reactions, and cyclization reactions. Additionally, 4,5-Dichloro-2-(methylthio)pyrimidine is utilized in the development of new materials and compounds with specific properties, making it a valuable tool in modern chemical research and innovation.