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273-33-6 (2H-[1,2,3]三唑并[4,5-B]吡啶,2H-1,2,3-Triazolo[4,5-b]pyridine)

结构式：

2H-[1,2,3]三唑并[4,5-B]吡啶结构式图片|273-33-6结构式图片

2H-[1,2,3]三唑并[4,5-B]吡啶MOL文件

CAS号：

273-33-6

中文名称：

2H-[1,2,3]三唑并[4,5-B]吡啶

英文名称：

2H-1,2,3-Triazolo[4,5-b]pyridine

分子式：

C₅H₄N₄

分子量：

120.112059593201

2H-[1,2,3]三唑并[4,5-B]吡啶(273-33-6)名称与标识符

名称

中文别名：

2H-[1,2,3]三唑并[4,5-B]吡啶;

英文别名：

2H-1,2,3-Triazolo[4,5-b]pyridine;DTXCID60104235;SY052565;I10125;1H-1,2,3-Triazolo4,5-bpyridine;1,2,3 triazolo[4,5-b]pyridine;1,2,3-Triazolo(5,4-b)pyridine;NSC-64288;3H-triazolo[4,5-b]pyridine;1H-[1,2,3]triazolo[4,5-b]pyridine;BDBM50591490;AKOS016002711;4-Azabenzotriazole;NSC 64288;InChI=1/C5H4N4/c1-2-4-5(6-3-1)8-9-7-4/h1-3H,(H,6,7,8,9);1H-triazolo[4,5-b]pyridine;MFCD00134183;SCHEMBL8321356;273-33-6;T1367;3H-Pyrido[2,3-d]-v-triazole;AC-27929;2H-triazolo[4,5-b]pyridine;AE-842/30158002;1H-1,2,3-Triazolo[4,5-b]pyridine;CS-0155695;AS-49414;SCHEMBL179848;NSC64288;273-34-7;Z3235024586;DTXSID20181744;1H-1,2,3-Triazolo[4,5-b]pyridine, 98%;3H-1,2,3-Triazolo[4,5-b]pyridine;SCHEMBL40861;VQNDBXJTIJKJPV-UHFFFAOYSA-;626-564-3;7-azabenzotriazole;CHEMBL2398101;2H-[1,2,3]triazolo[4,5-b]pyridine;3H-[1,2,3]Triazolo[4,5-b]pyridine;AKOS015892303;1H-1,2,3-Triazolo(4,5-b)pyridine;

标识符

InChIKey：

VQNDBXJTIJKJPV-UHFFFAOYSA-N

Inchi：

1S/C5H4N4/c1-2-4-5(6-3-1)8-9-7-4/h1-3H,(H,6,7,8,9)

SMILES：

C12=NNN=C1C=CC=N2

2H-[1,2,3]三唑并[4,5-B]吡啶(273-33-6)物化性质

计算特性

精确分子量 : 120.043596145Da
氢键供体数量 : 1
氢键受体数量 : 3
可旋转化学键数量 : 0
同位素质量 : 120.043596145Da
重原子数量 : 9
复杂度 : 105
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） : 0.3
拓扑分子极性表面积 : 54.5Å²

2H-[1,2,3]三唑并[4,5-B]吡啶(273-33-6)相关文献

1. Triazolopyridines as ligands: structural diversity in iron(ii), cobalt(ii), nickel(ii) and copper(ii) complexes of 3-(2-pyridyl)-[1,2,4]triazolo[4,3-a]pyridine (L10) and spin crossover in [FeII(L10)2(NCS)2]
Julia Klingele,Dominic Kaase,Jakob Hilgert,Gunther Steinfeld,Marco H. Klingele,Jochen Lach Dalton Trans. 2010 39 4495
2. H-bonding promotion of peptide solubility and cyclization by fluorinated alcohols
Hiroshi Hinou,Kei Hyugaji,Fayna Garcia-Martin,Shin-Ichiro Nishimura,Fernando Albericio RSC Adv. 2012 2 2729
3. The elimination of an alkoxy group in the photo-Graebe–Ullmann conversion of 1-(2,5-dialkoxyphenyl)triazolopyridines into carbolines, and the preparation of α-, γ- and δ-carboline quinones
Lina K. Mehta,John Parrick,Fereshteh Payne J. Chem. Soc. Perkin Trans. 1 1993 1261
4. Multicolor-tunable room-temperature afterglow and circularly polarized luminescence in chirality-induced coordination assemblies
Hui Liu,Dan-Dan Ren,Peng-Fu Gao,Kun Zhang,Ya-Pan Wu,Hong-Ru Fu,Lu-Fang Ma Chem. Sci. 2022 13 13922
5. The impact of 1,2,3-triazoles in the design of functional coatings
Sasidhar Kantheti,Ramanuj Narayan,K. V. S. N. Raju RSC Adv. 2015 5 3687
6. Natural polyenic macrolactams and polycyclic derivatives generated by transannular pericyclic reactions: optimized biogenesis challenging chemical synthesis
Rosana Alvarez,Angel R. de Lera Nat. Prod. Rep. 2021 38 1136
7. Silver(i)-mediated oxidative C(sp3)–H amination of ethers with azole derivatives under mild conditions
Xiaoyu Wu,Kai Qiao,Hong Qin,Dong Zhang,Di Gao,Zhao Yang,Zheng Fang,Kai Guo Org. Chem. Front. 2019 6 2672
8. PET imaging of tumours with a 64Cu labeled macrobicyclic cage amine ligand tethered to Tyr3-octreotate
Brett M. Paterson,Peter Roselt,Delphine Denoyer,Carleen Cullinane,David Binns,Wayne Noonan,Charmaine M. Jeffery,Roger I. Price,Jonathan M. White,Rodney J. Hicks,Paul S. Donnelly Dalton Trans. 2014 43 1386
9. Green and sustainable visible light-mediated formation of amide bonds: an emerging niche in organic chemistry
Jitender Singh,Anuj Sharma New J. Chem. 2022 46 16220
10. Charged chiral derivatization for enantioselective imaging of d-,l-2-hydroxyglutaric acid using ion mobility spectrometry/mass spectrometry
Eiji Sugiyama,Yuki Nishiya,Kenji Yamashita,Ryo Hirokawa,Yoshiteru Iinuma,Takashi Nirasawa,Hajime Mizuno,Yoshitaka Hamashima,Kenichiro Todoroki Chem. Commun. 2023 59 10916

目录

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问答

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