1. Home
  2. 5-Quinolinol, 2-chloro-

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)-

5-Quinolinol, 2-chloro-

Clc1ccc2c(n1)cccc2O Request for Quotation
Chemical Name: 5-Quinolinol, 2-chloro-
CAS Number: 124467-35-2
Product Number: AG000M2B(AGN-PC-0O0PCK)
Synonyms:
MDL No:
Molecular Formula: C9H6ClNO
Molecular Weight: 179.6030

Identification/Properties

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

Request for Quotation

Customer Feedback

Chemical Structure


2-Chloroquinolin-5-ol plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable reagent in the preparation of various organic compounds. This compound is commonly utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its ability to undergo a variety of chemical transformations, such as substitution, addition, and cyclization reactions, allows for the efficient construction of complex molecular structures. In particular, 2-Chloroquinolin-5-ol is frequently employed in the development of bioactive molecules and research compounds due to its pharmacological significance. Its presence in the chemical toolbox enables chemists to access diverse molecular scaffolds and explore new synthetic pathways for the creation of innovative compounds.