25192-03-4

Basic information

• Product Name: N-(1-ADAMANTYL)URETANE
• Synonyms: N-(1-ADAMANTYL)URETANE;ethyl N-(adamantan-1-yl)carbamate
• CAS NO: 25192-03-4
• Molecular Formula: C₁₃H₂₁NO₂
• Molecular Weight: 223.31
• Product Categories: Adamantane derivatives
• Mol File: 25192-03-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(1-ADAMANTYL)URETANE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-ADAMANTYL)URETANE(25192-03-4)
• EPA Substance Registry System: N-(1-ADAMANTYL)URETANE(25192-03-4)

Safety Data

• Hazardous Substances Data: 25192-03-4(Hazardous Substances Data)

Upstream product

• 281-23-2 adamantane 
• 51-79-6 urethane 
• 64-17-5 ethanol 
• 254751-16-1 2-(((1s,3s)-adamantan-1-yl)amino)-2-oxoacetic acid 
• 768-94-5 1-Adamantanamine 
• 541-41-3 chloroformic acid ethyl ester 
• 590-28-3 potassium cyanate 
• 32314-61-7 1-nitroxyadamantane 

Downstream Products

• 54979-97-4 C₁₇H₂₂BrN₃O 
• 54979-96-3 C₁₇H₂₂ClN₃O 
• 26496-36-6 N-(adamantan-1-yl)hydrazinecarboxamide 

Relevant articles and documents

Urethanes synthesis from oxamic acids under electrochemical conditions

Urethane synthesis via oxidative decarboxylation of oxamic acids under mild electrochemical conditions is reported. This simple phosgene-free route to urethanes involves an in situ generation of isocyanates by anodic oxidation of oxamic acids in an alcoholic medium. The reaction is applicable to a wide range of oxamic acids, including chiral ones, and alcohols furnishing the desired urethanes in a one-pot process without the use of a chemical oxidant.

Adamantane derivatives, part III*: Synthesis of some aminoadamantanes as novel antitumor aqents

New series of 1-(1-adamantyl)semicarbazide 3a, 1-(1-adamantyl)-4-(4-substituted phenyl)semicarbazides 3b-e, 1-(1-adamantyl)-3-(substituted aminosulfonyl)ureas 5a-g, 1-(1-adamantyl)-4-(1-adamantylamino-methylene)-semicarbazide 7, 1-(1-adamantyl)-4-(1-adama