跳转至内容
Merck
CN

C5132

Sigma-Aldrich

咔唑

≥95% purity (GC), powder

别名:

二苯并吡咯; 二苯基吡咯

登录查看公司和协议定价


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

产品名称

咔唑, ≥95% (GC)

蒸汽压

400 mmHg ( 323 °C)

质量水平

方案

≥95% (GC)

表单

powder

技术

titration: suitable

颜色

white to tan

沸点

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

正在寻找类似产品? 访问 产品对比指南

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

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

428.0 °F - closed cup

闪点(°C)

220.0 °C - closed cup

个人防护装备

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

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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)
CARBAZOLE DERIVATIVES IN CANCER TREATMENT-A REVIEW.
Kanneti Naga M, et al.
World Journal of Pharmacy and Pharmaceutical Sciences (2015)
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
Shen H Tan et al.
Organic letters, 14(22), 5621-5623 (2012-10-31)
The racemic modification of the Aspidosperma alkaloid limaspermidine (1) has been prepared in ten steps including one involving a Raney-cobalt-mediated tandem reductive cyclization of nitrile 8 to give the tetracyclic system 9b. Compound (±)-1 has been converted over two steps
Isis E Mejías Carpio et al.
Nanoscale, 4(15), 4746-4756 (2012-07-04)
It is critical to develop highly effective antimicrobial agents that are not harmful to humans and do not present adverse effects on the environment. Although antimicrobial studies of graphene-based nanomaterials are still quite limited, some researchers have paid particular attention

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门