1. Home
  2. ethyl 5-bromoquinoline-3-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)-

ethyl 5-bromoquinoline-3-carboxylate

CCOC(=O)c1cnc2c(c1)c(Br)ccc2 Request for Quotation
Chemical Name: ethyl 5-bromoquinoline-3-carboxylate
CAS Number: 1383551-36-7
Product Number: AG0018MB(AGN-PC-0HLTSH)
Synonyms:
MDL No:
Molecular Formula: C12H10BrNO2
Molecular Weight: 280.1173

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Ethyl 5-bromoquinoline-3-carboxylate is a versatile chemical compound widely used in chemical synthesis applications. Its unique structure and properties make it a valuable building block in the creation of various organic compounds.This compound is frequently employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its bromoquinoline core provides functional groups that allow for further modification and integration into complex molecular structures.In organic synthesis, Ethyl 5-bromoquinoline-3-carboxylate serves as a crucial starting material for the development of novel compounds with diverse biological activities. Its presence in a reaction scheme can lead to the formation of bioactive molecules with potential therapeutic benefits.Chemists utilize this compound to introduce specific functionalities or motifs into target molecules, enabling the design and production of compounds with tailored properties. By incorporating Ethyl 5-bromoquinoline-3-carboxylate into synthetic routes, researchers can access a wide range of structurally diverse compounds for various applications.Overall, the strategic use of Ethyl 5-bromoquinoline-3-carboxylate in chemical synthesis enables the creation of innovative molecules that have the potential to impact fields such as medicine, agriculture, and materials science.