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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)-

Quinazoline, 4,6-dichloro-2-methyl-

Clc1ccc2c(c1)c(Cl)nc(n2)C Request for Quotation
Chemical Name: Quinazoline, 4,6-dichloro-2-methyl-
CAS Number: 338739-44-9
Product Number: AG007IL3(AGN-PC-035MRY)
Synonyms:
MDL No:
Molecular Formula: C9H6Cl2N2
Molecular Weight: 213.0633

Identification/Properties

Computed Properties
Molecular Weight:
213.061g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
211.991g/mol
Monoisotopic Mass:
211.991g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
189
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-Dichloro-2-methylquinazoline is a versatile compound widely utilized in chemical synthesis. One significant application of this compound is as a building block in the pharmaceutical industry. Its unique structure and reactivity make it an essential intermediate in the synthesis of various drugs and pharmaceutical compounds. By incorporating 4,6-Dichloro-2-methylquinazoline into a chemical reaction, chemists can modify its structure to create novel molecules with potential therapeutic properties. This compound serves as a valuable tool for drug discovery and development efforts, enabling the synthesis of diverse and complex chemical structures for potential medical applications. Additionally, 4,6-Dichloro-2-methylquinazoline can also be utilized in academic research settings for the design and synthesis of new chemical entities with improved biological activities. Its role in chemical synthesis highlights its importance in advancing the field of medicinal chemistry and drug design.