206-68-8 ((6H-Indolo[3,2,1-de][1,5]naphthyridine)

快速询单

结构式：

6H-Indolo[3,2,1-de][1,5]naphthyridineMOL文件

CAS号：

206-68-8

英文名称：

6H-Indolo[3,2,1-de][1,5]naphthyridine

分子式：

C₁₄H₁₀N₂

分子量：

206.242602825165

6H-Indolo[3,2,1-de][1,5]naphthyridine(206-68-8)名称与标识符

名称

英文别名：

6H-Indolo[3,2,1-de][1,5]naphthyridine;Canthin;Canthine;SCHEMBL11445424;UNII-77V6259LUA;DTXSID70486635;206-68-8;Q27266605;6H-Indolo(3,2,1-de)(1,5)naphthyridine;77V6259LUA;

标识符

InChIKey：

VYQRBKCKQCRYEE-UHFFFAOYSA-N

Inchi：

1S/C14H10N2/c1-2-6-13-10(4-1)11-7-8-15-12-5-3-9-16(13)14(11)12/h1-8H,9H2

SMILES：

N12CC=CC3C1=C(C=CN=3)C1C=CC=CC2=1

6H-Indolo[3,2,1-de][1,5]naphthyridine(206-68-8)物化性质

实验特性

PSA : 17.82

计算特性

精确分子量 : 206.0845
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 : 206.084398327g/mol
重原子数量 : 16
复杂度 : 312
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） : 2.8
拓扑分子极性表面积 : 17.8Å²

6H-Indolo[3,2,1-de][1,5]naphthyridine(206-68-8)相关文献

1. Rhodium-catalyzed pyridannulation of indoles with diazoenals: a direct approach to pyrido[1,2-a]indoles
Sudam Ganpat Dawande,Bapurao Sudam Lad,Sunitkumar Prajapati,Sreenivas Katukojvala Org. Biomol. Chem. 2016 14 5569
2. Oxidation of amine α-carbon to amide: a review on direct methods to access the amide functionality
P. Nagaraaj,V. Vijayakumar Org. Chem. Front. 2019 6 2570
3. Natural product inspired design and synthesis of β-carboline and γ-lactone based molecular hybrids
Dharmender Singh,Nisha Devi,Vipin Kumar,Chandi C. Malakar,Saloni Mehra,Sunita Rattan,Ravindra K. Rawal,Virender Singh Org. Biomol. Chem. 2016 14 8154
4. Fluorescent natural products as probes and tracers in biology
Romain Duval,Christophe Duplais Nat. Prod. Rep. 2017 34 161
5. The circular dichroism and absorption spectra of alkaloids containing the aniline chromophore. The absolute configuration of calycanthine
S. F. Mason,G. W. Vane J. Chem. Soc. B 1966 370
6. Recent progress in the chemistry of indole alkaloids and mould metabolites
J. E. Saxton Nat. Prod. Rep. 1987 4 591
7. The biosynthesis of folicanthine
D. G. O'Donovan,M. F. Keogh J. Chem. Soc. C 1966 1570
8. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
Minoru Ishikura,Takumi Abe,Tominari Choshi,Satoshi Hibino Nat. Prod. Rep. 2015 32 1389
9. Recent progress in the chemistry of indole alkaloids and mould metabolites
J. E. Saxton Nat. Prod. Rep. 1984 1 21
10. Proceedings of the Chemical Society. February 1960
Proc. Chem. Soc. 1960 37