41859-85-2

Basic information

• Product Name: Benzamide, N-[(4-hydroxyphenyl)methyl]-
• CAS NO: 41859-85-2
• Molecular Formula: C14H13NO2
• Molecular Weight: 227.263
• Mol File: 41859-85-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzamide, N-[(4-hydroxyphenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-[(4-hydroxyphenyl)methyl]-(41859-85-2)
• EPA Substance Registry System: Benzamide, N-[(4-hydroxyphenyl)methyl]-(41859-85-2)

Safety Data

• Hazardous Substances Data: 41859-85-2(Hazardous Substances Data)

Upstream product

• 1485-70-7 N-benzylbenzamide 
• 614-45-9 tert-Butyl peroxybenzoate 
• 696-60-6 4-aminomethylphenol 
• 34907-24-9 N-(p-Nitrobenzyl) benzamide 
• 32478-65-2 N-(4'-Aminobenzyl)benzamide 
• 98-88-4 benzoyl chloride 

Downstream Products

• 90446-56-3 N-(benzoyl)-3,5-bis(pyrrolidinylmethyl)-4-hydroxybenzylamine 

Relevant articles and documents

Spirooxazoline Synthesis by an Oxidative Dearomatizing Cyclization

Spirocyclic compounds are of increasing importance owing to their potential applications in the development of new pharmaceuticals. Herein, we describe a new, rapid access to rarely seen spirooxazolines utilizing an I(I)/I(III) reaction manifold. The scope of the cyclization using phenols and naphthols is described along with the stereoselective functionalization of the spirocycles. The application of this method to the formation of dihydrooxazines is also demonstrated.

Synthesis and Antiarrhythmic and Parasympatholytic Properties of Substituted Phenols. 2. Amides

Thirty amides patterned after the antiarrhythmic drug changrolin were synthesized and their antiarrhythmic and parasympatholytic activities were assessed. There was no correlation between antiarrhythmic and parasympatholytic activities. Several of the ami