1H-1,2,3-Triazolo[4,5-b]pyridine - CAS 273-34-7
Catalog: |
BB019535 |
Product Name: |
1H-1,2,3-Triazolo[4,5-b]pyridine |
CAS: |
273-34-7 |
Synonyms: |
2H-triazolo[4,5-b]pyridine |
IUPAC Name: | 2H-triazolo[4,5-b]pyridine |
Description: | 1H-1,2,3-Triazolo[4,5-b]pyridine (CAS# 273-34-7) is a useful research chemical. |
Molecular Weight: | 120.11 |
Molecular Formula: | C5H4N4 |
Canonical SMILES: | C1=CC2=NNN=C2N=C1 |
InChI: | InChI=1S/C5H4N4/c1-2-4-5(6-3-1)8-9-7-4/h1-3H,(H,6,7,8,9) |
InChI Key: | VQNDBXJTIJKJPV-UHFFFAOYSA-N |
Boiling Point: | 303.4 °C at 760 mmHg |
Density: | 1.472 g/cm3 |
Appearance: | Orange to brown powder or crystals |
MDL: | MFCD00134183 |
LogP: | 0.35290 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113501939-A | Novel pyridotriazole receptor and synthesis and application of luminescent polymer thereof | 20210826 |
CN-113264938-A | Imidazo [1,5-a ] pyrazine-8-amine compound, preparation method, pharmaceutical composition and application | 20210721 |
CN-113480455-A | Preparation method of mirabegron related substance and intermediate thereof | 20210719 |
CN-113429417-A | Method for preparing camptothecin and evans blue coupled amphiphilic compound | 20210717 |
CN-113476404-A | Self-assembled nano-vesicle medicine and preparation method and application thereof | 20210717 |
PMID | Publication Date | Title | Journal |
21544037 | 20110504 | Acylation of heteroaromatic amines: facile and efficient synthesis of a new class of 1,2,3-triazolo[4,5-b]pyridine and pyrazolo[4,3-b]pyridine derivatives | Molecules (Basel, Switzerland) |
17355619 | 20070313 | 2-Arylhydrazononitriles as building blocks in heterocyclic synthesis: A novel route to 2-substituted-1,2,3-triazoles and 1,2,3-triazolo[4,5-b]pyridines | Beilstein journal of organic chemistry |
16438521 | 20060203 | Synthesis of oligonucleotides with 3'-terminal 5-(3-acylamidopropargyl)-3'-amino-2',3'-dideoxyuridine residues and their reactivity in single-nucleotide steps of chemical replication | The Journal of organic chemistry |
Complexity: | 105 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 120.043596145 |
Formal Charge: | 0 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 120.043596145 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 54.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.3 |
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