1. Home
  2. 2-chloro-7-methoxyquinazoline

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)-

2-chloro-7-methoxyquinazoline

COc1ccc2c(c1)nc(nc2)Cl Request for Quotation
Chemical Name: 2-chloro-7-methoxyquinazoline
CAS Number: 953039-15-1
Product Number: AG00IIYU(AGN-PC-0ALHPG)
Synonyms:
MDL No:
Molecular Formula: C9H7ClN2O
Molecular Weight: 194.6177

Identification/Properties

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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Chloro-7-methoxyquinazoline is a key intermediate utilized in chemical synthesis processes for the production of various pharmaceuticals, agrochemicals, and functional organic materials. Its unique structural properties make it a valuable building block in the development of antiviral, antibacterial, and anticancer agents. This compound serves as a versatile starting material in the creation of diverse quinazoline derivatives with potential therapeutic and biological activities. Additionally, its reactivity and selectivity make it a pivotal component in the synthesis of complex molecules, enabling the design of novel compounds with targeted properties and functions. In research and industrial settings, 2-Chloro-7-methoxyquinazoline plays a crucial role in advancing the exploration of new chemical entities and drug discovery initiatives. Its strategic positioning as a synthetic intermediate underscores its significance in advancing the frontiers of chemical science and unlocking innovative solutions in the realm of molecular design and synthesis.