6336-34-1

Basic information

• Product Name: 4-(4-carbamoylphenoxy)benzamide
• CAS NO: 6336-34-1
• Molecular Formula: C₁₄H₁₂N₂O₃
• Molecular Weight: 256.261
• Mol File: 6336-34-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 488.8°Cat760mmHg
• Flash Point: 257.9°C
• Density: 1.298g/cm³
• CAS DataBase Reference: 4-(4-carbamoylphenoxy)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-carbamoylphenoxy)benzamide(6336-34-1)
• EPA Substance Registry System: 4-(4-carbamoylphenoxy)benzamide(6336-34-1)

Safety Data

• Hazardous Substances Data: 6336-34-1(Hazardous Substances Data)

Usage

General Description

4-(4-carbamoylphenoxy)benzamide is a chemical compound with the molecular formula C15H13N3O3. It is a benzamide derivative with a carbamoylphenoxy group attached to the benzene ring. 4-(4-carbamoylphenoxy)benzamide has potential biological activities, and it may be used in pharmaceutical research and drug development. Its exact role and applications are still being investigated, but it is believed to have potential as a therapeutic agent due to its chemical structure and properties. Additional research is needed to fully understand the potential uses and effects of 4-(4-carbamoylphenoxy)benzamide.

Upstream product

• 2215-89-6 oxybis(benzoic acid) 
• 623-00-7 4-bromobenzenecarbonitrile 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 2215-76-1 4-(4-formylphenoxy)benzaldehyde 
• 101-84-8 diphenylether 
• 7158-32-9 4,4'-bis(chlorocarbonyl)diphenyl oxide 

Downstream Products

• 2579-42-2 4,4'-oxy-bis-benzylamine; dihydrochloride 
• 2215-89-6 oxybis(benzoic acid) 

Relevant articles and documents

Design, synthesis and evaluation of potent and selective inhibitors of mono-(ADP-ribosyl)transferases PARP10 and PARP14

A series of diaryl ethers were designed and synthesized to discern the structure activity relationships against the two closely related mono-(ADP-ribosyl)transferases PARP10 and PARP14. Structure activity studies identified 8b as a sub-micromolar inhibito

An artificial receptor for the intermolecular and enantioselective formation of peptide sheets

Peptide strands coupled at the C terminus to bis[p(aminomethyl)phenyl] ether allow in CHCl3 solution association of lipophilic N-protected peptides with hydrogen bonds in the mode of antiparallel β-sheets; the enantioselectivity observed with a phenylalanine derivative is characterized by a binding constant ratio of around 15.