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Merck
CN

BCR158

苯并[c]吖啶

BCR®, certified reference material

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About This Item

经验公式(希尔记法):
C17H11N
CAS号:
分子量:
229.28
Beilstein:
154999
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

certified reference material

Agency

BCR®

制造商/商品名称

JRC

技术

HPLC: suitable
gas chromatography (GC): suitable

包装形式

neat

储存温度

2-8°C

SMILES字符串

c1ccc2nc3c(ccc4ccccc34)cc2c1

InChI

1S/C17H11N/c1-3-7-15-12(5-1)9-10-14-11-13-6-2-4-8-16(13)18-17(14)15/h1-11H

InChI key

OAPPEBNXKAKQGS-UHFFFAOYSA-N

分析说明

For more information please see:
BCR158

法律信息

BCR is a registered trademark of European Commission

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Eye Dam. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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J Molnar et al.
Anticancer research, 13(1), 263-266 (1993-01-01)
Effect of K- and L- molecular orbital regions on expression of antiplasmid and carcinogenic activity was studied with various benz[c]acridine derivatives, tricyclic compounds (acridine orange, phenothiazines) and dibenzoazepine (imipramine). Antiplasmid compounds showed the out-of-phase of molecular orbital in the L-region.
T Kurihara et al.
Anticancer research, 14(5A), 1811-1822 (1994-09-01)
Resonance energies, circuit resonance energies and bond currents of benz[c]acridines were calculated by Aihara's IRE theory. Consequently, it was shown that these compounds had very stable aromatic characters with positive resonance energies and that the resonance energies per pi-electron values
W Levin et al.
Cancer research, 43(10), 4625-4628 (1983-10-01)
Benz[c]acridine (B[c]ACR) and 12 of its derivatives, including the 5 metabolically possible trans-dihydrodiols, the diastereomeric bay-region diol-epoxides, 2 non-bay-region diol-epoxides, and the K-region arene oxide, were tested for tumor-initiating activity on mouse skin. A single topical application of 0.4 to
Benz[c]acridine.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 129-134 (1983-12-01)
J Molnár et al.
In vivo (Athens, Greece), 9(5), 463-468 (1995-09-01)
The endotoxin neutralizing effects of several phenothiazines, benzophenothiazines and Pentaglobin (control) were investigated by spectrophotometry, tumor necrosis factor (TNF) induction and the conventional Limulus test. In animal experiments, some beneficial effects of complex forming compounds were found, however, the compounds

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