diphenylcarbodiimide

diphenylcarbodiimide Suppliers list
Company Name: ChemStrong Scientific Co.,Ltd  
Tel: 0755-0755-66853366 13670046396
Email: sales@chem-strong.com
Products Intro: Product Name:N,N'-methanediylidenedianiline
CAS:622-16-2
Purity:95% HPLC Package:10mg;25mg;50mg;100mg
Company Name: Shaanxi DIDU pharmaceutical and Chemical Co., Ltd  
Tel: 15229059051
Email: 1027@dideu.com
Products Intro: Product Name:Diphenylcarbodiimide
CAS:622-16-2
Purity:99% Package:25kg
Company Name: Shandong Jiuyue Biological Technology Co., LTD  
Tel: 15553348166
Email: m15553348166@163.com
Products Intro: Product Name:diphenylcarbodiimide
CAS:622-16-2
Purity:97%+ Package:50g,500g,1kg,5kg,10kg,25kg
diphenylcarbodiimide Basic information
Product Name:diphenylcarbodiimide
Synonyms:diphenylcarbodiimide;Benzenamine, N,N-methanetetraylbis-;carbodiphenylimide;Bis(phenylimino)methane;N,N'-Diphenylcarbodiimide;N,N'-Diphenylmethanediimine;phenyl(phenyliminomethylene)amine;BenzenaMine,N,N'-Methanetetraylbis- or diphenyl carbodiiMide
CAS:622-16-2
MF:C13H10N2
MW:194.23
EINECS:210-721-4
Product Categories:
Mol File:622-16-2.mol
diphenylcarbodiimide Structure
diphenylcarbodiimide Chemical Properties
Melting point 169°C
Boiling point 320.68°C (rough estimate)
density 1.1579 (rough estimate)
refractive index 1.5014 (estimate)
EPA Substance Registry SystemBenzenamine, N,N'-methanetetraylbis- (622-16-2)
Safety Information
MSDS Information
diphenylcarbodiimide Usage And Synthesis
PreparationTriphenylphosphine (2.62 g, 0.01 mol) in THF (10 mL) was added dropwise to N,N'-diphenylthiourea (2.28 g, 0.01 mol) and diethyl azodicarboxylate (1.74 g, 0.01 mol) in THF (20 mL) at room temperature. After standing overnight, the solvent was removed under reduced pressure and the residue was extracted with light petroleum (bp 30–60 C°) to separate soluble material from the remainder. The light petroleum extract was concentrated and distilled to give diphenylcarbodiimide; bp 85–90 C°/ 0.2 mmHg, 1.27 g, 65%.
A further development of the method by immobilization of DEAD effects an easily separable (insoluble) and non-explosive reagent in Mitsunobu reactions. The methyl azodicarboxylate reagent immobilized on polystyrene 1742 functions well in Mitsunobu reactions and gives yields comparable to those obtained with soluble DEAD. Diphenylcarbodiimide was obtained in 41% yield.
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Synthesis Reference(s)The Journal of Organic Chemistry, 51, p. 2613, 1986 DOI: 10.1021/jo00363a046
Synthetic Communications, 7, p. 387, 1977 DOI: 10.1080/00397917708050769
diphenylcarbodiimide Preparation Products And Raw materials
Preparation Products1,2,3-TRIPHENYLGUANIDINE-->NISTC604455
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