3-Ethynylpyridine - CAS 2510-23-8
Catalog: |
BB018737 |
Product Name: |
3-Ethynylpyridine |
CAS: |
2510-23-8 |
Synonyms: |
3-ethynylpyridine |
IUPAC Name: | 3-ethynylpyridine |
Description: | 3-Ethynylpyridine (CAS# 2510-23-8) is a useful research chemical. |
Molecular Weight: | 103.12 |
Molecular Formula: | C7H5N |
Canonical SMILES: | C#CC1=CN=CC=C1 |
InChI: | InChI=1S/C7H5N/c1-2-7-4-3-5-8-6-7/h1,3-6H |
InChI Key: | CLRPXACRDTXENY-UHFFFAOYSA-N |
Boiling Point: | 83-84 °C30 mmHg (lit.) |
Melting Point: | 39-40 °C (lit.) |
Purity: | > 98.0 % (GC) (T) |
Density: | 1.02 g/cm3 |
Appearance: | Colorless to brownish low melting solid |
Storage: | Freezer |
MDL: | MFCD02177459 |
LogP: | 1.06290 |
GHS Hazard Statement: | H228 (100%): Flammable solid [Danger Flammable solids] |
Precautionary Statement: | P210, P240, P241, P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113248455-A | 3, 5-disubstituted isoxazole derivatives and synthesis method thereof | 20210525 |
CN-113292561-A | Compound with dipyrrolopyridine structure, preparation method and medical application | 20210522 |
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CN-112851566-A | Synthesis method of alpha-oxo-selenoamide derivative | 20210128 |
PMID | Publication Date | Title | Journal |
22825466 | 20120914 | Formation of higher-order structures of chiral poly(ethynylpyridine)s depending on size, temperature, and saccharide recognition | Organic & biomolecular chemistry |
22363937 | 20120404 | Copper(II)/phenanthroline-mediated CD-enhancement and chiral memory effect on a meta-ethynylpyridine oligomer | Chemical communications (Cambridge, England) |
21629899 | 20110714 | Copper(II)-mediated chiral helicity amplification and inversion of meta-ethynylpyridine polymers with metal coordination sites | Chemical communications (Cambridge, England) |
19360166 | 20090428 | Azacrown-attached meta-ethynylpyridine polymer: saccharide recognition regulated by supramolecular device | Chemical communications (Cambridge, England) |
17300931 | 20070401 | Design and synthesis of beta-methoxyacrylate analogues via click chemistry and biological evaluations | Bioorganic & medicinal chemistry letters |
Complexity: | 109 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 103.042199164 |
Formal Charge: | 0 |
Heavy Atom Count: | 8 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 103.042199164 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 12.9 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.1 |
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