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重要文件

361011

Sigma-Aldrich

1H-1,2,3-三唑并[4,5-b]吡啶

98%

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About This Item

經驗公式(希爾表示法):
C5H4N4
CAS號碼:
分子量::
120.11
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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化驗

98%

mp

208 °C (dec.) (lit.)

SMILES 字串

c1cnc2nn[nH]c2c1

InChI

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

InChI 密鑰

VQNDBXJTIJKJPV-UHFFFAOYSA-N

一般說明

1H-1,2,3-Triazolo[4,5-b]pyridine belongs to the class of triazolopyridine.[1] It reacts with europium under solvothermal conditions in pyridine to yield the homoleptic framework containing EuII centers that are icosahedrally coordinated by the 12 nitrogen atoms of six chelating ligands.[2] The surface-enhanced Raman (SER) spectra of 1H-1,2,3-triazolo[4,5-b]pyridine adsorbed on silver hydrosols is studied in the region 3500-100cm-1.[3]

應用

1H-1,2,3-Triazolo[4,5-b]pyridine (1,2,3-Triazolo(5,4-b)pyridine) may be used:
  • as starting reagent in the synthesis of 2,4,8,10-tetranitro-5H-pyrido[3″,2″:4′,5′] [1,2,3] triazolo [1′,2′:1,2] [1,2,3]- triazolo [5,4-b]-pyridin-6-ium inner salt[4]
  • in the pesticide synthesis[5]
  • as an entry to mesoionic heteropentalene derivatives[6]

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Chemical derivatization of glycans is a common strategy to increase the analytical performance of MALDI-MS-based glycan profiling techniques. Hydrazide, one of the most popular tags, offers important advantages including allowing purification-free procedures. Several hydrazides have thus been used for glycomics
The Chemistry of the [1, 2, 3] Triazolo [1, 5-a] pyridines: An Update.
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Advances in Heterocyclic Chemistry, 100, 195-252 (2010)
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A review of energetic materials synthesis.
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