Dicyclohexylurea

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Dicyclohexylurea

IUPAC name 1,3-dicyclohexylurea
Identifiers
	PubChem	4277
ChemSpider	4126^Y
ChEMBL	CHEMBL1458^Y
Jmol-3D images	Image 1
SMILES O=C(NC1CCCCC1)NC2CCCCC2
InChI InChI=1S/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16)^Y Key: ADFXKUOMJKEIND-UHFFFAOYSA-N^Y InChI=1/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16) Key: ADFXKUOMJKEIND-UHFFFAOYAR InChI=1S/C13H24N2O/c16-13(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2,(H2,14,15,16) Key: ADFXKUOMJKEIND-UHFFFAOYSA-N
Properties
Molecular formula	C₁₃H₂₄N₂O
Molar mass	224.34 g mol⁻¹
Melting point	230-233 °C
Hazards
MSDS	External MSDS
S-phrases	S24/25
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Dicyclohexylurea is an organic compound, specifically, a urea. It is the byproduct of the reaction of dicyclohexylcarbodiimide with amines or alcohols. It may be prepared by the reaction of cyclohexylamine and S,S-dimethyl dithiocarbonate.^[1]

References

↑ Man-kit Leung, Jun-Liang Lai, King-Hang Lau, Hsiao-hua Yu, and Hsiang-Ju Hsiao (1996). "S,S-Dimethyl Dithiocarbonate: A Convenient Reagent for the Synthesis of Symmetrical and Unsymmetrical Ureas". The Journal of Organic Chemistry 61 (12): 4175–4179. doi:10.1021/jo9522825. PMID 11667305.

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