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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)-

4-Chloro-7-hydroxyquinazolin-6-yl pivalate

O=C(C(C)(C)C)Oc1cc2c(Cl)ncnc2cc1O Request for Quotation
Chemical Name: 4-Chloro-7-hydroxyquinazolin-6-yl pivalate
CAS Number: 1145671-38-0
Product Number: AG000EPI(AGN-PC-0WAGMT)
Synonyms:
MDL No:
Molecular Formula: C13H13ClN2O3
Molecular Weight: 280.7069

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-7-hydroxyquinazolin-6-yl pivalate is a versatile compound commonly utilized in chemical synthesis as a key building block for creating a wide range of pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and reactivity, this compound serves as an essential intermediate in the synthesis of various bioactive molecules. Its functional groups enable it to participate in a variety of organic reactions, such as acylation, alkylation, and nucleophilic substitution, making it an indispensable tool for organic chemists. In particular, its pivaloyl ester moiety provides protection for the hydroxyquinazoline core during reactions, allowing for selective manipulation of different functional groups within a molecule. Consequently, 4-Chloro-7-hydroxyquinazolin-6-yl pivalate plays a vital role in the development of new therapeutic agents, agricultural chemicals, and advanced materials.