1. Home
  2. tert-butyl 7-formyl-3,4-dihydro-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 7-formyl-3,4-dihydro-2H-quinoline-1-carboxylate

O=Cc1ccc2c(c1)N(CCC2)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 7-formyl-3,4-dihydro-2H-quinoline-1-carboxylate
CAS Number: 943736-61-6
Product Number: AG00II3H(AGN-PC-059B2C)
Synonyms:
MDL No:
Molecular Formula: C15H19NO3
Molecular Weight: 261.3163

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The tert-Butyl 7-formyl-3,4-dihydroquinoline-1(2H)-carboxylate compound serves as a versatile building block in chemical synthesis processes. Its unique structure and reactivity make it a valuable intermediate for the creation of various organic compounds with diverse applications.In organic synthesis, tert-Butyl 7-formyl-3,4-dihydroquinoline-1(2H)-carboxylate can be used as a key starting material for the construction of complex molecules such as pharmaceuticals, agrochemicals, and materials. Its formyl group can participate in various chemical reactions, including condensation and reduction reactions, enabling the introduction of functional groups or modifications to the molecular scaffold.The presence of the tert-butyl group provides steric hindrance, which can influence the regioselectivity and stereochemistry of subsequent transformations. This can be particularly useful in controlling the outcome of multi-step synthesis pathways and enhancing the overall efficiency of the synthetic process.Overall, tert-Butyl 7-formyl-3,4-dihydroquinoline-1(2H)-carboxylate is a valuable tool for synthetic chemists seeking to access diverse chemical space and develop novel compounds with tailored properties for various applications in the field of chemistry.