1. Home
  2. tert-butyl 3,3-dimethyl-4-oxo-2H-quinoline-1-carboxylate

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)-

tert-butyl 3,3-dimethyl-4-oxo-2H-quinoline-1-carboxylate

O=C(N1CC(C)(C)C(=O)c2c1cccc2)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 3,3-dimethyl-4-oxo-2H-quinoline-1-carboxylate
CAS Number: 179898-81-8
Product Number: AG0027CH(AGN-PC-0434J4)
Synonyms:
MDL No:
Molecular Formula: C16H21NO3
Molecular Weight: 275.3428

Identification/Properties

Safety Information

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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The tert-Butyl 3,3-dimethyl-4-oxo-3,4-dihydroquinoline-1(2H)-carboxylate is a versatile compound that plays a crucial role in chemical synthesis. Its unique structure and reactivity make it a valuable building block for the creation of complex molecules in the field of organic chemistry.This compound can be utilized as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its presence in a reaction pathway can help to introduce specific functionalities or stereochemical elements into the final product. Additionally, the tert-Butyl 3,3-dimethyl-4-oxo-3,4-dihydroquinoline-1(2H)-carboxylate can serve as a protecting group for sensitive functional groups, ensuring selective reactions occur at desired positions within a molecule.Chemists rely on the unique structure and reactivity of this compound to achieve challenging synthetic transformations and to access novel chemical entities with potential applications in diverse fields.