84863-81-0

Basic information

• Product Name: 4-IODOPHENYLACETAMIDE
• Synonyms: 4-IODOPHENYLACETAMIDE;ACETAMIDE 2-(P-IODOPHENYL)-;BENZENEACETAMIDE, 4-IODO-;4-iodoBenzeneacetamide
• CAS NO: 84863-81-0
• Molecular Formula: C₈H₈INO
• Molecular Weight: 261.06
• Mol File: 84863-81-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-IODOPHENYLACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-IODOPHENYLACETAMIDE(84863-81-0)
• EPA Substance Registry System: 4-IODOPHENYLACETAMIDE(84863-81-0)

Safety Data

• Hazardous Substances Data: 84863-81-0(Hazardous Substances Data)

Upstream product

• 13329-40-3 4-Iodoacetophenone 
• 1798-06-7 (4-iodophenyl)acetic acid 
• 37051-38-0 4-Iodobenzeneacetyl chloride 
• 63349-52-0 methyl 4-iodophenylacetate 
• 591-50-4 iodobenzene 
• 98-80-6 phenylboronic acid 

Downstream Products

• 99184-27-7 (4-iodo-phenyl)-acetic acid-(2,2,2-trichloro-1-hydroxy-ethylamide) 
• 84863-95-6 3-Hydroxy-4-(4-iodo-phenyl)-pyrrole-2,5-dione 

Relevant articles and documents

The actual active species of sulfur-modified gold-supported palladium as a highly effective palladium reservoir in the suzuki-miyaura coupling

The actual active species of the recently developed sulfur-modified, gold-supported palladium material, S-modified Au-supported Pd (SAPd), with one of the lowest Pd-releasing levels and high recyclability in the Suzuki-Miyaura coupling, was investigated. Also, SAPd was found to work repeatedly as an excellent Pd reservoir for liquid-phase combinatorial synthesis. Copyright

Heterocyclic derivatives

Compounds of formula (I) wherein R1 is hydrogen or hydroxy; R2 is hydrogen; or R1 and R2 are joined together so that CR1 14 CR2 is a double bond; X is selected from --Ch2 CH

Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties

Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.