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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)-

ethyl 4,6-dichloro-2-methylsulfanylpyrimidine-5-carboxylate

CCOC(=O)c1c(Cl)nc(nc1Cl)SC Request for Quotation
Chemical Name: ethyl 4,6-dichloro-2-methylsulfanylpyrimidine-5-carboxylate
CAS Number: 959070-42-9
Product Number: AG003Q9K(AGN-PC-0JSHF0)
Synonyms:
MDL No: MFCD12828684
Molecular Formula: C8H8Cl2N2O2S
Molecular Weight: 267.1323

Identification/Properties

Properties
MP:
64-66℃
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
267.124g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
265.968g/mol
Monoisotopic Mass:
265.968g/mol
Topological Polar Surface Area:
77.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
221
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 4,6-dichloro-2-(methylthio)pyrimidine-5-carboxylate is a versatile compound widely utilized in chemical synthesis processes. This compound plays a crucial role in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various biologically active molecules.In chemical synthesis, Ethyl 4,6-dichloro-2-(methylthio)pyrimidine-5-carboxylate serves as a valuable building block for the production of pharmaceutical compounds, herbicides, and pesticides. Its unique structure allows for the introduction of functional groups at specific positions, enabling chemists to modify its properties and create diverse compounds with desired biological activities.Furthermore, Ethyl 4,6-dichloro-2-(methylthio)pyrimidine-5-carboxylate exhibits excellent reactivity and compatibility with a wide range of reaction conditions, making it a preferred choice for synthetic chemists aiming to streamline complex chemical transformations. Its inclusion in synthetic routes enables efficient access to target molecules with high purity and yield, accelerating the drug discovery and development process.Overall, Ethyl 4,6-dichloro-2-(methylthio)pyrimidine-5-carboxylate is an indispensable tool in chemical synthesis, offering researchers a versatile platform to access novel compounds with potential applications in pharmaceuticals, agriculture, and material science.