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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)-

7-Quinazolinecarboxylicacid, 4-chloro-

OC(=O)c1ccc2c(c1)ncnc2Cl Request for Quotation
Chemical Name: 7-Quinazolinecarboxylicacid, 4-chloro-
CAS Number: 942507-89-3
Product Number: AG0036PL(AGN-PC-07HAXB)
Synonyms:
MDL No:
Molecular Formula: C9H5ClN2O2
Molecular Weight: 208.6012

Identification/Properties

Properties
BP:
392.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
208.601g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
208.004g/mol
Monoisotopic Mass:
208.004g/mol
Topological Polar Surface Area:
63.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
237
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


4-Chloro-7-quinazolinecarboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. One of its key applications is as a building block in the creation of novel pharmaceutical compounds. By incorporating $name$ into synthetic pathways, chemists can access a diverse array of quinazoline derivatives that exhibit varied biological activities. Additionally, $name$ serves as a crucial intermediate in the development of agrochemicals, dyes, and specialty chemicals. Its unique structure and reactivity make it a valuable tool for researchers seeking to design and produce complex molecules with specific functionalities. In summary, the role of 4-Chloro-7-quinazolinecarboxylic acid in chemical synthesis extends far beyond its individual characteristics, offering a pathway to innovation and discovery in the field of organic chemistry.