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About This Item
実験式（ヒル表記法）:
C17H11N
CAS番号:
分子量:
229.28
Beilstein:
154999
MDL番号:
UNSPSCコード:
41116107
PubChem Substance ID:
NACRES:
NA.24
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グレード
certified reference material
認証
BCR®
メーカー／製品名
JRC
テクニック
HPLC: suitable
gas chromatography (GC): suitable
フォーマット
neat
保管温度
2-8°C
SMILES記法
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
アナリシスノート
For more information please see:
BCR158
BCR158
法的情報
BCR is a registered trademark of European Commission
シグナルワード
Danger
危険有害性情報
危険有害性の分類
Acute Tox. 4 Oral - Eye Dam. 1
保管分類コード
11 - Combustible Solids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
BCR158-100MG:
最新バージョンのいずれかを選択してください：
T Kurihara et al.
Anticancer research, 16(5A), 2757-2765 (1996-09-01)
In order to clarify the effects of methyl substitution on the carcinogenic activity, each resonance energy (RE) of benz[c]acridines, benzo[a]phenothiazines, chrysene, and their methyl derivatives was calculated by Aihara's TRE theory. Some correlations seem to exist between the values of
R L Chang et al.
Cancer research, 44(11), 5161-5164 (1984-11-01)
The tumorigenicity of benz[c]acridine (B[c]ACR) and a number of its derivatives, including the five metabolically possible transdihydrodiols, the diastereomeric bay-region diol-epoxides, two non-bay-region diol-epoxides, and the K-region 5,6-oxide, were assessed in newborn mice. A total dose of 0.50 or 1.05
K Satoh et al.
Anticancer research, 17(5A), 3553-3557 (1997-12-31)
Among 13 benz[c]acridines, six 7-methyl-substituted compounds (7-methylbenz[c]acridine, 7,9-dimethylbenz[c]acridine, 7,10-dimethylbenz[c]acridine, 7,11-dimethylbenz[c]acridine, 7,9,10-trimethylbenz[c]acridine, 7,9,11-trimethylbenz[c]acridine) were carcinogenic, while the other seven compounds (benz[c] acridine, 8-methylbenz[c]acridine, 9-methylbenz[c]acridine, 10-methylbenz[c]acridine, 11-methylbenz[c]acridine, 5,7-dimethylbenz[c]acridine, cis-5,6-dihydroxy-5,6-dihydrobenz[c]acridine) were inactive. Using both McLachlan-Hückel molecular orbital (McLachlan-HMO) and HMO methods, all the
N Motohashi et al.
Journal of chromatography, 643(1-2), 1-10 (1993-07-23)
Benz[c]acridine and many of its related compounds have been shown to exhibit carcinogenic activity. Unfortunately, these compounds are continually being found in many natural and environmental samples in widely divergent geographical locations. A review of chromatographic methods for mainly benz[c]acridine
Separation of methyl-substituted benz[c]acridines by reversed-phase high-performance thin-layer chromatography.
K Kamata et al.
Journal of chromatography, 396, 437-440 (1987-06-19)
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