81282-38-4

Basic information

• Product Name: N-diphenoxymethylene benzamide
• Synonyms: N-diphenoxymethylene benzamide
• CAS NO: 81282-38-4
• Molecular Weight: 317.344
• Mol File: 81282-38-4.mol

Chemical Properties

• CAS DataBase Reference: N-diphenoxymethylene benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-diphenoxymethylene benzamide(81282-38-4)
• EPA Substance Registry System: N-diphenoxymethylene benzamide(81282-38-4)

Safety Data

• Hazardous Substances Data: 81282-38-4(Hazardous Substances Data)

Upstream product

• 108-95-2 phenol 
• 3911-55-5 N-benzoyl-carbonimidic acid dichloride 

Downstream Products

• 112758-46-0 1-Benzoyl-3-[2-(1-methyl-1H-imidazol-2-ylmethylsulfanyl)-ethyl]-2-phenyl-isourea 
• 565446-50-6 1-benzoyl-2-phenyl-3-[3-(1-trityl-1H-imidazol-4-yl)-propyl]-isourea 
• 150760-42-2 methyl 5E-6-(3-(benzoylimido-phenoxymethylenamino)phenyl)-6-(3-pyridyl)hex-5-enoate 
• 169266-33-5 N-<(phenoxy)(2,2,2-trifluoroethylamino)methylene>benzamide 
• 112758-47-1 1-Benzoyl-2-phenyl-3-[2-(2-pyridin-2-yl-1H-imidazol-4-ylmethylsulfanyl)-ethyl]-isourea 
• 106467-33-8 1-Benzoyl-2-phenyl-3-{3-[2-(tetrahydro-pyrimidin-2-ylideneamino)-thiazol-4-yl]-propyl}-isourea 
• 106467-30-5 1-Benzoyl-2-phenyl-3-{2-[2-(tetrahydro-pyrimidin-2-ylideneamino)-thiazol-4-ylmethylsulfanyl]-ethyl}-isourea 
• 112767-34-7 1-Benzoyl-3-{2-[2-(4-chloro-benzyl)-5-methyl-1H-imidazol-4-ylmethylsulfanyl]-ethyl}-2-phenyl-isourea 
• 112767-33-6 1-Benzoyl-3-[2-(5-methylsulfanyl-1H-imidazol-4-ylmethylsulfanyl)-ethyl]-2-phenyl-isourea 
• 106670-35-3 1-Benzoyl-3-[2-(naphthalen-2-ylmethylsulfanyl)-ethyl]-2-phenyl-isourea 
• 112758-49-3 1-Benzoyl-3-[2-(2-dimethylaminomethyl-thiazol-4-ylmethylsulfanyl)-ethyl]-2-phenyl-isourea 

Relevant articles and documents

IMIDAZOLYL ALKYL GUANIDINE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL PREPARATIONS CONTAINING THESE COMPOUNDS

New imidazolylalkyl-guanidine derivatives are described, which by virtue of their agonistic action on histamine-H 2 receptors and in part also due to their additional H 1-antagonistic receptor activity can be used in the treatment of cardiac diseases, certain forms of hypertension and diseases of arterial occlusion.These imidazolylalkyl-guanidine derivatives correspond to the general formula I: STR1

Structure of N-(Dialkoxymethylene)amides: Crystal Structure Analysis, Quantum Mechanical Calculations, and Spectroscopic Investigations

The title compounds 1 were synthesized either by acylation of the imidocarbonates 7 or by reaction of N-(dichloromethylene)benzamide (9) with phenols.The X-ray analysis of the dibromo derivative 1e indicates a s-cisoid gauche conformation of the central O