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Merck
CN

C5132

Sigma-Aldrich

咔唑

≥95% purity (GC), powder

别名:

二苯并吡咯; 二苯基吡咯

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About This Item

经验公式(希尔记法):
C12H9N
CAS号:
分子量:
167.21
Beilstein:
3956
EC 号:
MDL编号:
UNSPSC代码:
12171500
PubChem化学物质编号:
NACRES:
NA.47

product name

咔唑, ≥95% (GC)

蒸汽压

400 mmHg ( 323 °C)

质量水平

检测方案

≥95% (GC)

形式

powder

颜色

white to tan

bp

355 °C (lit.)

mp

243-246 °C (lit.)

溶解性

acetone: 50 mg/mL

密度

1.1 g/cm3 at 18 °C

应用

diagnostic assay manufacturing
hematology
histology

储存温度

room temp

SMILES字符串

c1ccc2c(c1)[nH]c3ccccc23

InChI

1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H

InChI key

UJOBWOGCFQCDNV-UHFFFAOYSA-N

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一般描述

咔唑是一种芳香族杂环有机分子。

应用

咔唑已用于糖醛酸的测定。

生化/生理作用

咔唑主要与 DNA 相互作用并对其造成损伤。这些事件可抑制新 DNA 或 RNA 的合成。咔唑衍生物具有抗微生物、抗肿瘤、抗癫痫、抗组胺、抗氧化、抗炎、抗腹泻、镇痛、神经保护和胰脂肪酶抑制活性。

质量

其可能含有黑色颗粒物。

象形图

Health hazard

警示用语:

Warning

危险声明

危险分类

Aquatic Chronic 4 - Carc. 2 - Muta. 2

WGK

WGK 2

闪点(°F)

428.0 °F

闪点(°C)

220.0 °C

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

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在文件库中查找您最近购买产品的文档。

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CARBAZOLE DERIVATIVES IN CANCER TREATMENT-A REVIEW.
Kanneti Naga M, et al.
World Journal of Pharmacy and Pharmaceutical Sciences (2015)
A complete set of hyaluronan fragments obtained from hydrolysis catalyzed by hyaluronidase: Application to studies of hyaluronan mass distribution by simple HPLC devices.
Tranchepain F, et al.
Analytical Biochemistry, 348, 232-242 (2006)
Guodong Ji et al.
Journal of hazardous materials, 225-226, 1-7 (2012-05-23)
We examined the effects of power and treatment time on the ultrasonically enhanced ozonation of carbazole dissolved in APG(1214) surfactant solutions, including an analysis of the mechanism of OH radical formation, the zeta potential of the colloidal suspension, the influence
Yuji Ashikawa et al.
BMC structural biology, 12, 15-15 (2012-06-26)
Dihydroxylation of tandemly linked aromatic carbons in a cis-configuration, catalyzed by multicomponent oxygenase systems known as Rieske nonheme iron oxygenase systems (ROs), often constitute the initial step of aerobic degradation pathways for various aromatic compounds. Because such RO reactions inherently
Jong-Kwan Bin et al.
Advanced materials (Deerfield Beach, Fla.), 24(21), 2911-2915 (2012-05-03)
A new carbazole derivative with two carbazole moieties on the C3 and C6 positions of carbazole and triphenylsilane directly linked to the N of carbazole is successfully used as a highly efficient blue phosphorescent host in an organic light-emitting diode

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