64407-57-4

Basic information

• Product Name: 1,1-dicyclohexylurea
• Synonyms: 1,1-dicyclohexylurea
• CAS NO: 64407-57-4
• Molecular Formula: C₁₃H₂₄N₂O
• Molecular Weight: 224.34
• Mol File: 64407-57-4.mol
• Article Data: 205

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,1-dicyclohexylurea(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-dicyclohexylurea(64407-57-4)
• EPA Substance Registry System: 1,1-dicyclohexylurea(64407-57-4)

Safety Data

• Hazardous Substances Data: 64407-57-4(Hazardous Substances Data)

Upstream product

• 151-51-9 carbodiimide 
• 15535-98-5 p-hydroxybenzamidine 
• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 
• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 70-54-2 2,6-diaminocaproic acid 
• 134-32-7 1-amino-naphthalene 
• 37642-93-6 4-(naphthalene-1-ylamino)-4-oxo-butanoic acid 
• 73427-55-1 7-guanidinoheptanoic acid 
• 344407-83-6 4-Phenylbutylphosphonous acid 

Downstream Products

• 281660-19-3 2,4-hexadienyl-2,4-dihydroxy benzoate 
• 281660-18-2 2,4-hexadienyl-4-hydroxy benzoate 
• 1541-19-1 ethyl N-cyclohexylcarbamate 

Relevant articles and documents

Self-assembly and micellization of a dual thermoresponsive supramolecular pseudo-block copolymer

This paper reports the studies on self-assembly and thermosensitive micellization phenomena of a supramolecular polymeric host-guest system consisting of star-shaped poly(N-isopropylacrylamide) (PNIPAAm) with a β-cyclodextrin (β-CD) core (the host polymer

METHOD FOR THE IMMOBILIZATION OF BIOMOLECULES

The invention relates to a method for the immobilization of biomolecules containing at least one sulfhydryl group, which method comprises contacting a modified metal surface with the biomolecule irradiating the resulting surface with UV radiation in the presence of a photo-initiator, wherein said metal surface is modified with a cross-linker compound comprising a terminal thiol or dithiol group covalently linked to the metal surface, a spacer group, which at the other terminal end is carrying an isolated double or triple bond.

New fatty acid derivatives based on barbiturates and other cyclic β-dicarbonyl compounds and an acyl migration

The use of DCC, triethylamine and 4-dimethylaminopyridine in dichloromethane provides a general and standard one-pot procedure for the O-acylation of cyclic β-dicarbonyl compound derivatives (1) with palmitic and stearic acids which have long hydrocarbon tails, to synthesis of new type of fatty acid derivative in good to excellent yields. Structure elucidation was carried out by FT-IR, 1H NMR and 13C NMR spectroscopy techniques. The acyl migration was also found in results and the corresponding structure was characterized by X-ray crystallography. A proposed mechanism was discussed for the formation of products.