ProphetesAI is thinking...
pyridine
Answers
MindMap
Loading...
Sources
Pyridine - Wikipedia
Pyridine is a basic heterocyclic organic compound with the chemical formula C 5 H 5 N . It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom (=N−). It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.
en.wikipedia.org
en.wikipedia.org
Pyridine - PubChem
Pyridine is a colorless liquid with an unpleasant smell. It can be made from crude coal tar or from other chemicals. Pyridine is used to dissolve other ...
pubchem.ncbi.nlm.nih.gov
pubchem.ncbi.nlm.nih.gov
Pyridine - American Chemical Society
Pyridine is a colorless liquid with a foul odor and several hazardous properties. In the late 1840s, physician/chemist Thomas Anderson at the University of ...
www.acs.org
www.acs.org
pyridine
pyridine Chem. (ˈpɪrɪdiːn) [f. Gr. πῦρ, πυρ- fire + -id4 + -ine5.] a. A colourless volatile liquid alkaloid (C5H5N) of offensive odour and poisonous quality, produced in the dry distillation of bone-oil and other bituminous matter. The inhalation of its vapour was said to be beneficial in asthma, et...
Oxford English Dictionary
prophetes.ai
Pyridine anhydrous, 99.8 110-86-1 - Sigma-Aldrich
Pyridine may be used as a base for the conversion of: Alkyltrichlorosilanes to trimethoxyalkylsilanes, which are used as precursors for preparing ...
www.sigmaaldrich.com
www.sigmaaldrich.com
NIOSH Pocket Guide to Chemical Hazards - Pyridine - CDC
Colorless to yellow liquid with a nauseating, fish-like odor ... Molecular Weight ... 79.1 ... Boiling Point ... 240°F ... Freezing Point ... 44°F ... Solubility ... Miscible.
www.cdc.gov
www.cdc.gov
Pyridine (data page)
This page provides supplementary chemical data on pyridine.
wikipedia.org
en.wikipedia.org
PYRIDINE | CAMEO Chemicals | NOAA
A clear colorless to light yellow liquid with a penetrating nauseating odor. Vapors are heavier than air. Toxic by ingestion and inhalation.
cameochemicals.noaa.gov
cameochemicals.noaa.gov
Skeletal editing of pyridines to aryldialdehydes - Nature
Pyridine skeletal editing can generally be categorized into two main types (Fig. 1A). One type focuses on the skeletal editing of pyridine into ...
www.nature.com
www.nature.com
Pyridine - an overview | ScienceDirect Topics
Pyridine is a heterocyclic compound in which a carbon atom of benzene is exchanged with nitrogen.
www.sciencedirect.com
www.sciencedirect.com
CHEBI:16227 - pyridine - EMBL-EBI
ChEBI Name, pyridine. ChEBI ID, CHEBI:16227. Definition, An azaarene comprising a benzene core in which one -CH group is replaced by a ...
www.ebi.ac.uk
www.ebi.ac.uk
Pyridine-4-carbaldehyde
The other isomers are pyridine-2-carboxaldehyde and pyridine-3-carboxaldehyde. Pyridine-4-carboxaldehyde is a colorless liquid, although aged samples can appear yellow or even brown.
wikipedia.org
en.wikipedia.org
Dichlorotetrakis(pyridine)iron(II)
Dichlorotetrakis(pyridine)iron(II) is the coordination complex with the formula FeCl2(pyridine)4. CoCl2(pyridine)4 and NiCl2(pyridine)4. It is prepared by treating ferrous chloride with an excess of pyridine.
wikipedia.org
en.wikipedia.org
Chichibabin pyridine synthesis
The Chichibabin pyridine synthesis () is a method for synthesizing pyridine rings. See also
Chichibabin reaction
Gattermann–Skita synthesis
Hantzsch pyridine synthesis
Ciamician–Dennstedt rearrangement
References
Pyridine forming reactions
wikipedia.org
en.wikipedia.org
Pyridine alkaloids
Pyridine alkaloids are a class of alkaloids, nitrogen-containing chemical compounds widely found in plants, that contain a pyridine ring. Alkaloids with a pyridine partial structure are usually further subdivided according to their occurrence and their biogenetic origin.
wikipedia.org
en.wikipedia.org