N,N'-Dicyclohexylcarbodiimide Suppliers, N,N'-Dicyclohexylcarbodiimide Manufacturers.
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N,N'-Dicyclohexylcarbodiimide
Category :
Organic chemicals and Derivatives/OthersSynonyms :
DCC;Dicyclohexyl CARBODIMIDE;Dicyclohexylcarbodiimide;N,N'-Dicyclohexyl carbodiimide;N,N'-Dicyclohexylcarbodimide;N,N'-diphenylcarbodiimide;N,N-dicyclohexylcarbodiimide;N,N-dicyclohexyl carbodiimide;N,N'-dicyclohexyl carbodimide;CAS NO :
538-75-0EC NO :
208-704-1Molecular Formula :
C13H22N2Molecular Weight :
206.33Main Specifications :
In-houseInChI :
InChI=1/C13H10N2/c1-3-7-12(8-4-1)14-11-15-13-9-5-2-6-10-13/h1-10HPacking :
25 kg/drumProduct description :
Purity by GC: ≥99.0% Certification: ISO 9001; Application: Its primary use is to couple amino acids during artificial peptide synthesis. DCC has been used in the preparation of titanate nanotubes-phthalocyanine(TiONts-Pc) nanohybrids and 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-yl propynoate. DCC may be used to promote the esterification of 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-ol with propiolic acid to form 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-yl propynoate. It can also used to synthesize: • 1,3-Thiazetedine derivatives via [2+2] cycloaddition with 2-phenylethenyl- and 2-(4-itrophenyl)ethenyl isothiocyanates. • 1,3,5-Oxadiazine-4-thiones via [4+2] cycloaddition with benzoyl isothiocyanates. • Sterically hindered 1,3,4-oxadiazole derivatives by reacting with (N- isocyanimino)triphenylphosphorane in the presence of aromatic (or heteroaromatic) carboxylic acids.Uses :
Coupling Agent/ Dehydrating AgentMolecular Structure :
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