1. Home
  2. Quinazoline, 4-chloro-7-methoxy-

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)-

Quinazoline, 4-chloro-7-methoxy-

COc1ccc2c(c1)ncnc2Cl Request for Quotation
Chemical Name: Quinazoline, 4-chloro-7-methoxy-
CAS Number: 55496-52-1
Product Number: AG00I9WM(AGN-PC-022OWS)
Synonyms:
MDL No:
Molecular Formula: C9H7ClN2O
Molecular Weight: 194.6177

Identification/Properties

Properties
MP:
141 - 142 °C
BP:
323°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
194.618g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
194.025g/mol
Monoisotopic Mass:
194.025g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
179
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-Chloro-7-methoxyquinazoline, a versatile compound used in chemical synthesis, is a key building block in the creation of various pharmaceuticals, agrochemicals, and materials. With its unique structure and reactivity, this compound serves as a key intermediate in the synthesis of biologically active molecules, aiding in the development of new drugs and compounds with diverse applications. Its presence in the synthesis process facilitates the formation of important molecular structures, allowing for the creation of compounds with specific properties and functions. In the realm of chemical synthesis, 4-Chloro-7-methoxyquinazoline plays a crucial role in the development of advanced materials and compounds that contribute to various industries and scientific research endeavors.