65037-30-1

Basic information

• Product Name: [bis-(p-chlorobenzoyloxy)iodo]benzene
• Synonyms: [bis-(p-chlorobenzoyloxy)iodo]benzene
• CAS NO: 65037-30-1
• Molecular Weight: 515.131
• Mol File: 65037-30-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: [bis-(p-chlorobenzoyloxy)iodo]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: [bis-(p-chlorobenzoyloxy)iodo]benzene(65037-30-1)
• EPA Substance Registry System: [bis-(p-chlorobenzoyloxy)iodo]benzene(65037-30-1)

Safety Data

• Hazardous Substances Data: 65037-30-1(Hazardous Substances Data)

Upstream product

• 932-72-9 (Dichloroiodo)benzene 
• 74-11-3 para-chlorobenzoic acid 
• 591-50-4 iodobenzene 
• 3240-34-4 [bis(acetoxy)iodo]benzene 

Downstream Products

• 1242065-24-2 1-methyl-4-nitroso-4-piperidinyl 4-chlorobenzoate 
• 1871-38-1 phenyl 4-chlorobenzoate 

Relevant articles and documents

Preparation method and device for iodobenzene dibenzoate derivative

The invention relates to a preparation method and device for an iodobenzene dibenzoate derivative. The method includes the steps that 6 mmol of iodobenzene diacetate and 12 mmol of benzoic acid or a benzoic acid derivative or pivalic acid are added into a

α-Acyloxynitroso dienophiles in [4+2] hetero Diels-Alder cycloadditions: mechanistic insights

α-Acyloxynitroso derivatives are a class of heterodienophiles leading to valuable 3,6-dihydro-1,2-oxazines or the corresponding aminoalcohols in good yields. The discovery that a β-oxygenated moiety led to a domino [4+2] cycloaddition/σN-O bond cleavage in the presence of a catalytic amount of Lewis acid was investigated in detail, through kinetic profiling of the reaction both in the absence and presence of a promoter. These studies showed that the role of the Lewis acid was to accelerate the σN-O bond cleavage thereby promoting a highly reproducible sequence. In addition, our preliminary results on an asymmetric version of this domino sequence are reported.