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Merck

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號碼:
MDL號碼:
分類程式碼代碼:
12171500
PubChem物質ID:
NACRES:
NA.47

product name

咔唑, ≥95% (GC)

蒸汽壓力

400 mmHg ( 323 °C)

品質等級

化驗

≥95% (GC)

形狀

powder

顏色

white to tan

bp

355 °C (lit.)

mp

243-246 °C (lit.)

溶解度

acetone: 50 mg/mL

密度

1.1 g/cm3 at 18 °C

應用

diagnostic assay manufacturing
hematology
histology

儲存溫度

room temp

SMILES 字串

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 密鑰

UJOBWOGCFQCDNV-UHFFFAOYSA-N

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一般說明

咔唑是一种芳香族杂环有机分子。

應用

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。

品質

其可能含有黑色颗粒物。

象形圖

Health hazard

訊號詞

Warning

危險聲明

危險分類

Aquatic Chronic 4 - Carc. 2 - Muta. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

428.0 °F - closed cup

閃點(°C)

220.0 °C - closed cup

個人防護裝備

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


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CARBAZOLE DERIVATIVES IN CANCER TREATMENT-A REVIEW.
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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)
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
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
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

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