Merck
CN
所有图片(1)

文件

P19809

Sigma-Aldrich

2-苯基苯并咪唑

97%

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经验公式（希尔记法）:
C13H10N2
CAS号:
716-79-0
分子量:
194.23
EC 号:
211-939-2
MDL编号:
MFCD00005592
eCl@ss:
32151902
PubChem化学物质编号:
24898258
NACRES:
NA.22

检测方案

97%

形式

solid

mp

293-296 °C (lit.)

SMILES字符串

c1ccc(cc1)-c2nc3ccccc3[nH]2

InChI

1S/C13H10N2/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9H,(H,14,15)

InChI key

DWYHDSLIWMUSOO-UHFFFAOYSA-N

基因信息

human ... FGFR1(2260) , PDGFRB(5159)

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相关类别

象形图

CorrosionExclamation mark
GHS05,GHS07

警示用语：

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Mehrorang Ghaedi et al.
Journal of hazardous materials, 158(1), 131-136 (2008-03-04)
A new and efficient solid phase extraction method is described for the preconcentration of trace heavy metal ions. The method is based on the adsorption of Fe(3+), Cu(2+) and Zn(2+) on 2-phenyl-1H-benzo[d] imidazole (PHBI) loaded on Triton X-100-coated polyvinyl chloride
Yukio Kubota et al.
Nucleic acids research. Supplement (2001), (2)(2), 193-194 (2003-08-09)
We have studied the influence of terminal substituents, amidinium group and N-methylpiperazine ring, of 2-phenylbenzimidazole compounds (1-6; Figure 1) on their DNA-binding modes. Experimental results reveal that 1-3 are accepted in intercalation pockets owing to structural flexibility of the N-methylpiperazine
Charity N Mosley et al.
International journal of environmental research and public health, 4(2), 126-131 (2007-07-10)
2-phenylbenzimidazole (PBI) is an ingredient found in sunscreen agents. PBI can absorb the UV portion of the solar light and undergo a series of light-induced reactions to cause adverse effects in humans. Therefore, chemical and photochemical toxicity of PBI were
J Johnson Inbaraj et al.
Photochemistry and photobiology, 75(2), 107-116 (2002-03-09)
The sunscreen agent 2-phenylbenzimidazole-5-sulfonic acid (PBSA) and its parent 2-phenylbenzimidazole (PBI) cause DNA photodamage via both Type-I and Type-II mechanisms when UVB irradiated. We have studied the photophysical and photochemical properties of these compounds and their ability to photogenerate reactive
Shirley Cruz Lio et al.
Cancer chemotherapy and pharmacology, 61(6), 1045-1058 (2007-08-11)
Cancer chemotherapy continues to be challenged by the emergence of resistant tumors, and one organelle entwined in the development of drug resistance is the Golgi apparatus. Recently, we discovered a group of 2-(substituted phenyl)-benzimidazole (2-PB) compounds that displace resident Golgi
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