1. Home
  2. 1-chloro-7-(trifluoromethyl)isoquinoline

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

1-chloro-7-(trifluoromethyl)isoquinoline

Clc1nccc2c1cc(cc2)C(F)(F)F Request for Quotation
Chemical Name: 1-chloro-7-(trifluoromethyl)isoquinoline
CAS Number: 1196154-02-5
Product Number: AG000PCA(AGN-PC-0CH9A2)
Synonyms:
MDL No:
Molecular Formula: C10H5ClF3N
Molecular Weight: 231.6016

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


1-Chloro-7-(trifluoromethyl)isoquinoline is a versatile compound that finds application in chemical synthesis as a valuable building block. This compound serves as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure and reactivity make it an ideal starting material for the preparation of complex molecules through diverse synthetic strategies. The chloro and trifluoromethyl substituents on the isoquinoline scaffold allow for selective functionalization and modification, enabling the creation of novel molecules with tailored properties. In organic synthesis, 1-Chloro-7-(trifluoromethyl)isoquinoline plays a crucial role in the development of new materials, agrochemicals, and bioactive compounds. Its versatility and compatibility with a wide range of synthetic methods make it a valuable tool for chemists seeking to access structurally intricate and biologically relevant molecules.