V900131
1,1′-羰基二咪唑
Vetec™, reagent grade, 97%
别名:
CDI
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关于此项目
经验公式（希尔记法）:
C7H6N4O
化学文摘社编号:
分子量:
162.15
EC Number:
208-488-9
UNSPSC Code:
12352115
PubChem Substance ID:
Beilstein/REAXYS Number:
6826
MDL number:
InChI key
PFKFTWBEEFSNDU-UHFFFAOYSA-N
InChI
1S/C7H6N4O/c12-7(10-3-1-8-5-10)11-4-2-9-6-11/h1-6H
SMILES string
O=C(n1ccnc1)n2ccnc2
grade
reagent grade
product line
Vetec™
assay
97%
mp
117-122 °C (lit.)
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Application
CDI可用于：
- 使丙二酸衍生物脱羧生成羰基咪唑部分，可进一步与不同的亲核试剂反应。
- 活化纤维素膜，用于免疫传感器应用。
- 对Fe3O4-SiO2核壳纳米颗粒进行功能化，用于生物应用。
- 通过与顺式和反式1，2-氨基醇反应制备顺式和反式1，2-咪唑基丙胺。
- 制备N-取代咪唑衍生物，进一步制备新型离子液体。
Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Synthesis and surface functionalization of Fe3O4-SiO2 core-shell nanoparticles with 3-glycidoxypropyltrimethoxysilane and 1, 1′-carbonyldiimidazole for bio-applications
Ta TKH, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 504(2), 376-383 (2016)
1, 1′-Carbonyldiimidazole mediates the synthesis of N-substituted imidazole derivatives from Morita--Baylis--Hillman adducts
Rodrigues Jr MT, et al.
Tetrahedron Letters, 55(1), 180-183 (2014)
Regio-and Stereospecific Syntheses of syn-and anti-1, 2-Imidazolylpropylamines from the Reaction of 1, 1′-Carbonyldiimidazole with syn-and anti-1, 2-Amino Alcohols
Mulvihill MJ, et al.
The Journal of Organic Chemistry, 69(15), 5124-5127 (2004)
Daniela Stöllner et al.
Analytical biochemistry, 304(2), 157-165 (2002-05-16)
Methods for the activation of a cellulose dialysis membrane for immunosensor applications have been developed. For activation two reagents, 1,1'-carbonyldiimidazole (CDI) and 1-cyano-4-dimethylaminopyridinium tetrafluoroborate (CDAP), were compared with respect to the coupling efficiency for glucose oxidase (GOx) and 1,8-diamino-2,6-dioxaoctane. The
Thomas-Xavier Métro et al.
Chemical communications (Cambridge, England), 48(96), 11781-11783 (2012-10-31)
The synthesis of various amides has been realised avoiding the use of any organic solvent from activation of carboxylic acids with CDI to isolation of the amides. Mechanochemistry was the key point of the process allowing rapid formation of the
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