69805-79-4

Basic information

• Product Name: N-benzyl-N’,N’-morpholinylurea
• Synonyms: N-benzyl-N’,N’-morpholinylurea
• CAS NO: 69805-79-4
• Molecular Weight: 220.271
• Mol File: 69805-79-4.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: N-benzyl-N’,N’-morpholinylurea(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-N’,N’-morpholinylurea(69805-79-4)
• EPA Substance Registry System: N-benzyl-N’,N’-morpholinylurea(69805-79-4)

Safety Data

• Hazardous Substances Data: 69805-79-4(Hazardous Substances Data)

Upstream product

• 110-91-8 morpholine 
• 69805-66-9 benzylcarbamic acid 1,1,4-trioxo-2,5-diphenyl-4,5-dihydro-1H-1λ⁶-thiophen-3-yl ester 
• 121820-08-4 Benzyl-carbamic acid 3,5-dioxo-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-4-yl ester 
• 6976-49-4 morpholine-4-carboxylic acid ethyl ester 
• 100-46-9 benzylamine 
• 4257-83-4 benzyl 2,2,2-trichloroacetamide 
• 88333-03-3 Benzyl isocyanide 
• 33054-04-5 phenylacetyl azide 
• 103-82-2 phenylacetic acid 
• 1530-89-8 N-cyanomorpholine 
• 100-51-6 benzyl alcohol 
• 93605-74-4 4-[(1H-imidazol-1-yl)carbonyl]morpholine 
• 25180-84-1 N-benzylmorpholine-4-carbothioamide 
• 124-38-9 carbon dioxide 

Relevant articles and documents

N-functionalized benzotriazole-1-carboximidoyl chlorides: Synthetic equivalents for isocyanide dichlorides

Readily prepared N-functionalized benzotriazole-1-carboximidoyl chlorides are proposed as stable and novel isocyanide dichloride synthetic equivalents. Subsequent condensations of these new intermediates afford polysubstituted guanidines, S-aryl isothiour

METHOD OF CONVERTING CARBON DIOXIDE INTO CARBONYL COMPOUNDS

The present invention provides a method for fixing carbon dioxide gas as a carbonyl compound represented by formula (3) as depicted by Figure 1 and comprising, purging of carbon dioxide in a solution of a nucleophile represented by the formula (1) in presence of a solvent at a temperature ranging from -40 Degree Celsius to 35 Degree Celsius, followed by adding a reagent at temperature ranging from -40 degree to 35 degree and thereafter adding another nucleophile represented by the formula (2) to obtain carbonyl compound represented by formula (3). The present invention can be advantageously used to obtain commercially important carbonyl compounds and clean unwanted carbon dioxide gas from the atmosphere and industrial effluents.

A green, isocyanide-based three-component reaction approach for the synthesis of multisubstituted ureas and thioureas

A one-pot, isocyanide based multicomponent protocol was presented starting from secondary amines towards (thio)urea derivatives and utilized for the construction of a diverse 27-membered chemical library. Following a green compatible microwave assisted condition, the formed N,N′-multisubstituted (thio)ureas were obtained in up to 85% yield.