3-苯基咪唑并[1,5-a]吡啶 | 35854-46-7
3-苯基咪唑并[1,5-a]吡啶
3-Phenylimidazo1,5-apyridine
35854-46-7
C13H10N2
194.2319
名称和标识符
MDL |
MFCD00208500 |
InChIKey |
BLGGTXOVNVHSSV-UHFFFAOYSA-N |
Inchi |
1S/C13H10N2/c1-2-6-11(7-3-1)13-14-10-12-8-4-5-9-15(12)13/h1-10H |
SMILES |
N12C([H])=C([H])C([H])=C([H])C1=C([H])N=C2C1C([H])=C([H])C([H])=C([H])C=1[H] |
别名信息
- 中文别名 -
- 3-苯基咪唑并[1,5-a]吡啶
- 3-Phenylimidazo[1,5-a]pyridine 3-苯基咪唑并[1,5-a]吡啶
- 4'-甲氧基-2-联苯乙酸
- 英文别名 -
- 3-Phenylimidazo[1,5-a]pyridine
- 3-Phenyl-2,3a-diazaindene
- ACMC-209ijl
- 3-phenylimidazo<
- 1,5-a>
- pyridine
- Oprea1_737273
- 3-phenylimidazolo<
- 3,4-a>
- 3-phenyl-imidazo[1,5-a]pyridine
- Maybridge1_003584
- AC1LCTXL
- 3-Phenyl-imidazo[1,5-a]pyridin
- 3-Phenyl-imidazo<
- 1.5-a>
- pyridin
- Kinome_3407
- NULL
- 3-phenylimidazo<1,5-a>pyridine
- 3-phenylimidazolo<3,4-a>pyridine
- AI-204
- Imidazo[1,5-a]pyridine, 3-phenyl-
- Oprea1_802822
- MLS000851429
- HMS551K20
- BLGGTXOVNVHSSV-UHFFFAOYSA-N
- HMS2807H22
- 3-Phenylimidazo[1,5-a]pyridine #
- 3-phenyl-4-hydroimidazo[1,5-a]pyridine
- SMR000457872
- DP 01774
- ST50037935
- P1838
物化性质
实验特性
LogP |
3.00130 |
PSA |
17.30000 |
沸点 |
140°C/2mmHg(lit.) |
熔点 |
108.0 to 112.0 deg-C |
计算特性
精确分子量 |
194.08400 |
氢键供体数量 |
0 |
氢键受体数量 |
1 |
可旋转化学键数量 |
1 |
重原子数量 |
15 |
复杂度 |
211 |
拓扑分子极性表面积 |
17.3 |
相关文献
-
1.
Synthesis and biological evaluation of imidazo[1,5-a]pyridine-benzimidazole hybrids as inhibitors of both tubulin polymerization and PI3K/Akt pathway
Ahmed Kamal,A. V. Subba Rao,V. Lakshma Nayak,N. V. Subba Reddy,Konderu Swapna,G. Ramakrishna,Mallika Alvala Org. Biomol. Chem. 2014 12 9864
-
2.
Synthesis of imidazo[1,5-a]pyridines via I2-mediated sp3 C–H amination
Zhiyuan Hu,Jiao Hou,Jie Liu,Wenquan Yu,Junbiao Chang Org. Biomol. Chem. 2018 16 5653
-
3.
Iodide-promoted transformations of imidazopyridines into sulfur-bridged imidazopyridines or 1,2,4-thiadiazoles
Shi-Tang Ma,Xiao-Xiao Zhu,Jing-Yu Xu,Ying Li,Xiao-Mei Zhang,Cheng-Tao Feng,Yizhe Yan Chem. Commun. 2021 57 5338
-
4.
Iodide-promoted transformations of imidazopyridines into sulfur-bridged imidazopyridines or 1,2,4-thiadiazoles
Shi-Tang Ma,Xiao-Xiao Zhu,Jing-Yu Xu,Ying Li,Xiao-Mei Zhang,Cheng-Tao Feng,Yizhe Yan Chem. Commun. 2021 57 5338
-
5.
Iodine-catalyzed direct C–H thiolation of imidazo[1,5-a]quinolines for the synthesis of 3-sulfenylimidazo[1,5-a]quinolines
Song-Song Wu,Cheng-Tao Feng,Di Hu,Ye-Kai Huang,Zhong Li,Zai-Gang Luo,Shi-Tang Ma Org. Biomol. Chem. 2017 15 1680
-
6.
Imidazo[1,5-a]pyridine-1-ylalkylalcohols: synthesis via intramolecular cyclization of N-thioacyl 1,2-aminoalcohols and their silyl ethers and molecular structures
Toshiaki Murai,Eri Nagaya,Fumitoshi Shibahara,Toshifumi Maruyama Org. Biomol. Chem. 2012 10 4943
-
7.
Heterocyclic systems related to pyrrocoline. Part I. 2: 3a-Diazaindene
J. D. Bower,G. R. Ramage J. Chem. Soc. 1955 2834
-
8.
Recent synthetic methodologies for imidazo[1,5-a]pyridines and related heterocycles
Mittapalli Ramana Reddy,Chandra Mohan Darapaneni,Rajendra D. Patil,Harshita Kumari Org. Biomol. Chem. 2022 20 3440
-
9.
A novel approach for the synthesis of imidazo and triazolopyridines from dithioesters
Ajjahalli B. Ramesha,Nagarakere C. Sandhya,Chottanahalli S. Pavan Kumar,Mahanthawamy Hiremath,Kempegowda Mantelingu,Kanchugarakoppal S. Rangappa New J. Chem. 2016 40 7637
-
10.
Mg3N2-assisted one-pot synthesis of 1,3-disubstituted imidazo[1,5-a]pyridine
Suhas G. Patil,Jagannath S. Jadhav,Sagar T. Sankpal RSC Adv. 2020 10 11808
参考资料
Reaxys RN |
139649 |
Beilstein |
23(5)8,472 |
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