[1,2,4]triazolo[1,5-a]pyridine - CAS 274-85-1
Catalog: |
BB019585 |
Product Name: |
[1,2,4]triazolo[1,5-a]pyridine |
CAS: |
274-85-1 |
Synonyms: |
[1,2,4]triazolo[1,5-a]pyridine; [1,2,4]triazolo[1,5-a]pyridine |
IUPAC Name: | [1,2,4]triazolo[1,5-a]pyridine |
Description: | [1,2,4]triazolo[1,5-a]pyridine (CAS# 274-85-1) is a useful reactant in the synthesis of 1,2,4-triazolo[4,3-a]quinolines. |
Molecular Weight: | 119.127 |
Molecular Formula: | C6H5N3 |
Canonical SMILES: | C1=CC2=NC=NN2C=C1 |
InChI: | InChI=1S/C6H5N3/c1-2-4-9-6(3-1)7-5-8-9/h1-5H |
InChI Key: | DACWQSNZECJJGG-UHFFFAOYSA-N |
Density: | 1.29 g/cm3 |
MDL: | MFCD03700708 |
LogP: | 0.72930 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]; H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation] |
Precautionary Statement: | P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113121532-A | Preparation method of dye intermediate | 20210422 |
CN-112500397-A | Organic electroluminescent material with dibenzofuran-connected anthracene core structure and preparation method and device thereof | 20201218 |
WO-2021165834-A1 | 5-(3-(ethylsulfonyl)pyridin-2-yl)-pyrazolo[1,5-a]pyrimidine derivatives and related compounds as pesticide and insecticide agents for crop protection | 20200218 |
WO-2021159372-A1 | Use of jak inhibitors in preparation of drugs for treating jak kinase-related diseases | 20200213 |
WO-2021160109-A1 | Dihydronaphthyridinone compound, and preparation method therefor and medical use thereof | 20200213 |
PMID | Publication Date | Title | Journal |
22594690 | 20120614 | A selective, orally bioavailable 1,2,4-triazolo[1,5-a]pyridine-based inhibitor of Janus kinase 2 for use in anticancer therapy: discovery of CEP-33779 | Journal of medicinal chemistry |
22509764 | 20120510 | Novel 1,2,4-triazolo[1,5-a]pyridines and their fused ring systems attenuate oxidative stress and prolong lifespan of Caenorhabiditis elegans | Journal of medicinal chemistry |
22011201 | 20111118 | Rearrangement of aryl- and benzylthiopyridinium imides with participation of a methyl substituent | The Journal of organic chemistry |
19095445 | 20090201 | DNA gyrase (GyrB)/topoisomerase IV (ParE) inhibitors: synthesis and antibacterial activity | Bioorganic & medicinal chemistry letters |
Complexity: | 105 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 119.048347172 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 119.048347172 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 30.2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.7 |
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