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CAS No 530-62-1 , di(imidazol-1-yl)methanone Search by region : Switzerland

  • Name: di(imidazol-1-yl)methanone
  • Synonyms: Carbonyldiimidazole;di(imidazol-1-yl)methanone; N,N'-Carbonyldiimidazole; Carbonyl diimidazole; N,N-Carbonyldiimidazole; 530-62-1; 1,1'-Carbonylbis-1H-imidazole;1,1'-Carbonyldiimidazole;
  • CAS Registry Number:
  • Transport: UN 3263 8/PG 2
  • Melting Point: 118-120 ºC
  • Density: 1.39 g/cm3
  • Refractive index: 1.665
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • HS Code: 29332990
  • EINECS: 208-488-9
  • Molecular Weight: 162.14874
  • InchiKey: PFKFTWBEEFSNDU-UHFFFAOYSA-N
  • InChI: InChI=1S/C7H6N4O/c12-7(10-3-1-8-5-10)11-4-2-9-6-11/h1-6H
  • Risk Statements: S26;S37/39
  • Molecular Formula: C7H6N4O
  • Molecular Structure:CAS No:530-62-1 di(imidazol-1-yl)methanone

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530-62-1 N,N-CARBONYLDIIMIDAZOLE (CDI)

  • Switzerland DKSH Switzerland Ltd. [Manufacturer]
  • Tel: +41 44 386 72 72
  • Fax: +41 44 386 72 82
  • Address:

    DKSH Switzerland Ltd.
    Wiesenstrasse 8 / P.O. Box 888
    8034 Zurich/Switzerland null,nullSwitzerland

Contact Supplier

530-62-1 1,1''-CARBONYLDIIMIDAZOLE

  • Switzerland CONNECT MARKETING GMBH [Manufacturer]
  • Tel: +41 81 740 58 50
  • Fax: +41 81 740 58 51
  • Address: CONNECT MARKETING GMBH
    BAHNWEG NORD 35
    CH-9475 SEVELEN/SG
    SWITZERLAND null,nullSwitzerland
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References of di(imidazol-1-yl)methanone
Title: N,N-Carbonyldiimidazole
CAS Registry Number: 530-62-1
CAS Name: 1,1¢-Carbonylbis-1H-imidazole
Molecular Formula: C7H6N4O
Molecular Weight: 162.15
Percent Composition: C 51.85%, H 3.73%, N 34.55%, O 9.87%
Literature References: Prepd from phosgene and imidazole in dry tetrahydrofuran or dry benzene: Staab, Ann. 609, 75 (1957); Anderson, Paul, J. Am. Chem. Soc. 80, 4423 (1958).
Properties: Crystals from tetrahydrofuran or benzene, mp 115.5-116°. Should be handled under exclusion of atmospheric moisture. Hydrolyzed by water in a few sec with evolution of CO2.
Melting point: mp 115.5-116°
Use: In the synthesis of peptides. Reacts readily with carboxylic acids to form acyl imidazoles; subsequent reaction with amines to form amides goes smoothly.