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Merck
CN

705284

Sigma-Aldrich

1,1′-羰基二咪唑 溶液

0.4 M in methylene chloride

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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
Beilstein:
6826
MDL编号:
UNSPSC代码:
12352115
PubChem化学物质编号:
NACRES:
NA.22
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表单

liquid

反应适用性

reaction type: Carbonylations

浓度

0.4 M in methylene chloride

折射率

n20/D 1.434

密度

1.303 g/mL at 25 °C

SMILES字符串

O=C(n1ccnc1)n2ccnc2

InChI

1S/C7H6N4O/c12-7(10-3-1-8-5-10)11-4-2-9-6-11/h1-6H

InChI key

PFKFTWBEEFSNDU-UHFFFAOYSA-N

一般描述

1,1′-Carbonyldiimidazole (N,N′-carbonyldiimidazole) is a versatile peptide-forming reagent.

应用

1,1′-Carbonyldiimidazole (N,N′-carbonyldiimidazole) may be used in the following studies:
  • Synthesis of peptides in aqueous solution.
  • Synthesis of isoleucine-5 angiotensin II amide-1.
  • For the activation of the hydroxyl termini of tween toward nucleophilic addition.
  • As coupling reagent for the coupling of prostaglandins and other carboxylic acids to the amino groups of bovine serum albumin.
  • Synthesis of peptide thioesters.

警示用语:

Danger

危险声明

危险分类

Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

靶器官

Central nervous system

储存分类代码

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Robert J Chen et al.
Proceedings of the National Academy of Sciences of the United States of America, 100(9), 4984-4989 (2003-04-17)
Novel nanomaterials for bioassay applications represent a rapidly progressing field of nanotechnology and nanobiotechnology. Here, we present an exploration of single-walled carbon nanotubes as a platform for investigating surface-protein and protein-protein binding and developing highly specific electronic biomolecule detectors. Nonspecific
Zain Kassam et al.
Inflammatory bowel diseases, 20(12), 2483-2492 (2014-09-05)
Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC) is perceived to harbor significant morbidity but limited excess mortality, thought to be driven by colon cancer, compared with the general population. Recent studies suggest mortality rates seem
N,N'-carbonyldiimidazole-induced peptide formation in aqueous solution.
K W Ehler et al.
Biochimica et biophysica acta, 434(1), 233-243 (1976-05-20)
N, N'-Carbonyldiimidazole in Peptide Synthesis. III. 1 A Synthesis of Isoleucine-5 Angiotensin II Amide-I.
Paul R and Anderson GW.
The Journal of Organic Chemistry, 27(6), 2094-2099 (1962)
N,N'-carbonyldiimidazole as coupling reagent for the preparation of bovine serum albumin conjugates.
U Axen
Prostaglandins, 5(1), 45-47 (1974-01-10)

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