119411-68-6

Basic information

• Product Name: C₉H₆BrClO
• Synonyms: C₉H₆BrClO
• CAS NO: 119411-68-6
• Molecular Weight: 245.503
• Mol File: 119411-68-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: C₉H₆BrClO(CAS DataBase Reference)
• NIST Chemistry Reference: C₉H₆BrClO(119411-68-6)
• EPA Substance Registry System: C₉H₆BrClO(119411-68-6)

Safety Data

• Hazardous Substances Data: 119411-68-6(Hazardous Substances Data)

Upstream product

• 6630-33-7 ortho-bromobenzaldehyde 
• 7345-79-1 2-bromocinnamic acid 

Downstream Products

• 1217485-03-4 (E)-3-(2-bromophenyl)-N-[4-methyl-3-(4-pyridin-3-ylpyrimidin-2-ylamino)phenyl]acrylamide 

Relevant articles and documents

The synthesis of 3,4-disubstituted dihydroquinolin-2(1H)-one under metal-free conditions in aqueous solution

A novel route toward 3,4-disubstituted dihydroquinolin-2(1H )-ones via radical process has been developed in aqueous solution without metals. This method offers a new and simple route for the synthesis of skeleton of dihydroquinolin-2(1H )-one in one step

1,4-Palladium Shift/C(sp3)-H Activation Strategy for the Remote Construction of Five-Membered Rings

1,n-Metal shift is an elegant alternative approach enabling the functionalization of remote C-H bonds from simple precursors. In this work, we report a novel and simple Pd0-catalyzed domino reaction involving 1,4-palladium shift and C(sp3)-H activation and leading to (fused) five-membered rings. This method allowed access to a broad range of valuable arylidene γ-lactams and indanones and was applied to the formal synthesis of (-)-pyrrolam.

Silver-catalyzed radical tandem cyclization for the synthesis of 3,4-disubstituted dihydroquinolin-2(1 H)-ones

A silver-catalyzed tandem decarboxylative radical addition/cyclization of N-arylcinnamamides with aliphatic carboxylic acids is reported. This method affords a novel and straightforward route to various 3,4-disubstituted dihydroquinolin-2(1H)-ones in aque