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1,2,7,8-二苯并吖啶 | 224-42-0

1,2,7,8-二苯并吖啶结构式图片|224-42-0结构式图片
1,2,7,8-二苯并吖啶
Dibenza,jacridine
224-42-0
C21H13N
279.34
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:1,2,7,8-二苯并吖啶结构式
9177
名称和标识符
MDL MFCD00055947
InChIKey ANUCHZVCBDOPOX-UHFFFAOYSA-N
Inchi InChI=1S/C21H13N/c1-3-7-16-14(5-1)9-11-20-18(16)13-19-17-8-4-2-6-15(17)10-12-21(19)22-20/h1-13H
SMILES C1=CC=C2C(=C1)C=CC3=NC4=C(C=C23)C5=CC=CC=C5C=C4
别名信息
- 中文别名 -
  • 1,2,7,8-二苯并吖啶
  • 二苯并(a,j)丫啶
  • Di苯并(a,j)acridine,neat 标准品
  • 二苯并(a,j)吖啶 标准品
  • 二苯(a,j)吖啶
  • 二苯并吖啶
  • 二苯并(A,J)丫啶
- 英文别名 -
  • 1,2,7,8-Dibenzacridine
  • Dibenz[a,j]acridine
  • Dibenzo(a,j)ac
  • Dibenz(a,j)acridine
  • Dibenz(a,j)acridine Solution
  • 1,2,7,8-Dibenzacridin
  • Dibenzacridine
  • Dibenzo<aj>acridin
  • 1,8-Dibenzacridine
  • Dibenz[a,j]acridine, BCR(R) certified Reference Material
  • 3,5,6-Dibenzacridine
  • 3,4,6,7-Dinaphthacridine
  • Dibenz(a,f)acridine
  • 1.2,7,8-Dibenzacridin
  • DIBENZ(A,J)ACRIDINE [HSDB]
  • Dibenz[a,j]acridine
  • 1,2:7,8-Dibenzacridine
  • 7-Azadibenz[a,j]anthracene
  • NSC 114903
  • CCRIS 207
  • DB(a,j)AC
  • FT-0624625
  • 088X9K64S8
  • 13-azapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene
  • 3,6,7-Dinaphthacridine
  • Dibenz[a,f]acridine
  • 224-42-0
  • Dibenzo[a,j]acridine
  • Q26840806
  • NSC-114903
  • SCHEMBL604812
  • NSC114903
  • 13-azapentacyclo[12.8.0.03, 12.04, 9.017, 22]docosa-1(14), 2, 4, 6, 8, 10, 12, 15, 17, 19, 21-undecaene
  • DIBENZ (a,j) ACRIDINE (purity)
  • 1,7,8-Dibenzacridine
  • DTXSID4059758
  • NSC 114903
  • UNII-088X9K64S8
  • DIBENZ(A,J)ACRIDINE
  • 7-Azadibenz[a,j]anthracene
  • J-014720
  • DIBENZ(A,J)ACRIDINE [IARC]
  • 1,2:7,8-Dibenzacridine
  • C19220
  • HSDB 4036
  • 7-Azadibenz(a,j)anthracene
  • 13-azapentacyclo[12.8.0.0?,??.0?,?.0??,??]docosa-1,3(12),4,6,8,10,13,15,17,19,21-undecaene
  • ANUCHZVCBDOPOX-UHFFFAOYSA-N
  • Dibenz(a,j)acridine, vial of 25 mg, analytical standard
  • BRN 0018508
  • CS-0450092
  • NS00014412
  • WLN: T E6 D6 B666 NNJ
  • CHEBI:82311
物化性质
实验特性
LogP 5.69440
PSA 12.89000
折射率 1.8240 (estimate)
沸点 412.11°C (rough estimate)
熔点 218-220°C
蒸气压 0.0±1.4 mmHg at 25°C
闪点 240.3±14.1 °C
颜色与性状 No data avaiable
密度 1.0343 (rough estimate)
计算特性
精确分子量 279.10500
氢键供体数量 0
氢键受体数量 1
可旋转化学键数量 0
同位素质量 279.104799
重原子数量 22
复杂度 369
同位素原子数量 0
确定原子立构中心数量 0
不确定原子立构中心数量 0
确定化学键立构中心数量 0
不确定化学键立构中心数量 0
共价键单元数量 1
疏水参数计算参考值(XlogP) 6
互变异构体数量
表面电荷 0
拓扑分子极性表面积 12.9
海关数据
海关编码 2933990090
海关数据

中国海关编码:

2933990090

概述:

2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

申报要素:

品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期

Summary:

2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

相关文献
  • 1. Carcinogenic nitrogen compounds. Part LXXI. Acridines from 5-aminobenzo[b]selenophen
    N. P. Buu-Ho?,M. Dufour,P. Jacquignon,M. Renson,G. Maréchal,A. Ruwet J. Chem. Soc. C 1971 2308
  • 2. Dibenzoacridines: synthesis by alkyne–carbonyl-metathesis and properties
    Erich Ammon,Paul Heine,Miguel Andre Argüello Cordero,Stefan Lochbrunner,Alexander Villinger,Peter Ehlers,Peter Langer Org. Biomol. Chem. 2023 21 4504
  • 3. Carcinogenic nitrogen compounds. Part LXXXIII. New condensed acridines derived from benz[c]indeno[1,3-mn]-, benz[c]indeno[1,3-kl]-, and phenanthro[9,10,1-mna]-acridines
    P. Jacquignon,O. Périn-Roussel J. Chem. Soc. Perkin Trans. 1 1973 2311
  • 4. Carcinogenic nitrogen compounds. Part LIII. Thiazole isosteres of dibenzacridines and dibenzocarbazoles
    N. P. Buu-Ho?,A. Martani,A. Ricci,M. Dufour,P. Jacquignon,G. Saint-Ruf J. Chem. Soc. C 1966 1790
  • 5. Carcinogenic nitrogen compounds. Part LIV. Some limitations to the Bernthsen synthesis of meso-substituted benzacridines
    N. P. Buu-Ho?,P. Jacquignon,M. Dufour,M. Mangane J. Chem. Soc. C 1966 1792
  • 6. Carcinogenic nitrogen compounds. Part LXXIII. Cyclisation of 12-(o-chloroaryl)benz[a]acridines: a route to new condensed acridines derived from naphtho[2,1,8-def]quinoline (1-azapyrene)
    N. P. Buu-Ho?,O. Périn-Roussel,P. Jacquignon J. Chem. Soc. Perkin Trans. 1 1972 234
  • 7. Highly site-selective alkylation reaction of bent aza-heterocycles by alkyllithium and alkyl halides
    Dipanjan Pan,Bidhan C. Roy,Gandhi K. Kar,Jayanta K. Ray J. Chem. Soc. Perkin Trans. 1 2000 2171
  • 8. Induction and inhibition of human cytochrome P4501 by oxygenated polycyclic aromatic hydrocarbons
    Emma Wincent,Florane Le Bihanic,Kristian Dreij Toxicol. Res. 2016 5 788
  • 9. Intermediates in the decomposition of aliphatic diazo-compounds. Part IX. Kinetics and mechanism of the decomposition of diaryldiazomethanes catalysed by zinc halides
    D. Bethell,K. C. Brown J. Chem. Soc. Perkin Trans. 2 1972 895
  • 10. Carcinogenic nitrogen compounds. Part LXX. Polycyclic naphthyridines by means of the Ullmann–Fetvadjian reaction
    N. P. Buu-Ho?,P. Jacquignon,M. Mangane J. Chem. Soc. C 1971 1991
专业数据库参考
PubChemId 9177
参考资料
Reaxys RN
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