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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)-

Pyrimidine, 4,6-bis(difluoromethoxy)-2-(methylthio)-

CSc1nc(OC(F)F)cc(n1)OC(F)F Request for Quotation
Chemical Name: Pyrimidine, 4,6-bis(difluoromethoxy)-2-(methylthio)-
CAS Number: 100478-25-9
Product Number: AG00022Z(AGN-PC-0NEXVT)
Synonyms:
MDL No:
Molecular Formula: C7H6F4N2O2S
Molecular Weight: 258.1934

Identification/Properties

Properties
MP:
48℃
BP:
302.442°C at 760 mmHg
Form:
Solid
Computed Properties
Molecular Weight:
258.191g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
5
Exact Mass:
258.009g/mol
Monoisotopic Mass:
258.009g/mol
Topological Polar Surface Area:
69.5A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
195
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

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Chemical Structure


4,6-Bis(difluoromethoxy)-2-(methylthio)pyrimidine is a versatile compound commonly utilized in chemical synthesis processes to introduce specific functional groups into target molecules. Its unique structure provides a valuable building block for the creation of complex organic compounds with enhanced properties and applications.This compound is particularly valuable in the pharmaceutical industry, where it is used as a key intermediate in the synthesis of various drug molecules. By incorporating 4,6-Bis(difluoromethoxy)-2-(methylthio)pyrimidine into the chemical reactions, chemists can modify the structure of pharmaceutical compounds to improve their potency, stability, or bioavailability.Moreover, in the field of material science, this compound plays a crucial role in the development of novel materials with tailored properties. Its presence in chemical reactions allows researchers to control the physical and chemical characteristics of materials, leading to the creation of advanced polymers, coatings, and other high-performance substances.Overall, 4,6-Bis(difluoromethoxy)-2-(methylthio)pyrimidine serves as a valuable tool for chemists and researchers seeking to expand the possibilities of chemical synthesis and create innovative compounds with diverse applications.