Pyridine-2-carbaldehyde - Wikipedia
Pyridine-2-carbaldehyde is a colorless oily liquid with a distinctive odor. Older samples are often brown-colored owing to impurities. It serves as a precursor to other compounds of interest in coordination chemistry and pharmaceuticals .
2-Pyridinecarboxaldehyde 99 1121-60-4 - MilliporeSigma
Aldrich-P62003; 2-Pyridinecarboxaldehyde 0.99; CAS No.: 1121-60-4; Synonyms: Picolinaldehyde; Pyridine-2-aldehyde; Linear Formula: C6H5NO; Empirical Formula: C6H5NO; find related products, papers, technical documents, MSDS & more at Sigma-Aldrich.
Pyridinecarboxaldehydes: Structures, Vibrational Assignments and ...
2023年2月3日 · The main focus of this article is on the structural, energetic and vibrational properties of three monosubstituted pyridines, wherein one of the hydrogen atoms of the pyridine is replaced by an aldehyde moiety.
2-Pyridinecarboxaldehyde - NIST Chemistry WebBook
Other names: Picolinaldehyde; 2-Pyridinealdehyde; Pyridine-2-carboxaldehyde; Pyridine-2-aldehyde; 2-Pyridylaldehyde; 2-Pyridinecarbaldehyde; α-Picolinaldehyde; o-Nicotinaldehyde; Picolinal; Picolinic aldehyde; 2-Formylpyridine; 2-Picolinaldehyde; 2-Picolinealdehyde; 2-Pyridaldehyde; 2-Pyridylcarboxaldehyde; NSC 8951; pyridine-2-carbaldehyde
2-Pyridinecarboxaldehyde | C6H5NO | CID 14273 - PubChem
An irritant that may cause serious eye injury; May cause skin sensitization; Harmful by ingestion; Toxic by inhalation; [Alfa Aesar MSDS] Search for (1121-60-4[EC/RN Number]) AND (sensitizer OR sensitization OR allergic) found no results; [PubMed) See Pyridine.
2-吡啶甲醛 - 百度百科
2-吡啶甲醛是一种有机化合物，分子式为C6H5NO。是有机磷酸酯类解毒药解磷定（PAM）和缓泻药比沙可啶（bisacodyl）的原料。
4-Pyridinecarboxaldehyde 97 872-85-5 - MilliporeSigma
A combined computational/experimental study on HSA binding of two water-soluble Schiff base ligands derived from pyridine derivative and ethylendiamine.
Pyridinecarbaldehyde - an overview | ScienceDirect Topics
The reaction proceeds by initial formation of an allyltin reagent that undergoes transmetallation with InCl 3 and, in general, proceeds to give the anti-product owing to an equatorial orientation of the aldehyde substituent in the six-membered transition state.
Pyridine - Wikipedia
The Hantzsch pyridine synthesis typically uses a 2:1:1 mixture of a β-keto acid (often acetoacetate), an aldehyde (often formaldehyde), and ammonia or its salt as the nitrogen donor. First, a double hydrogenated pyridine is obtained, which is then oxidized to the corresponding pyridine derivative.
4-Pyridinecarboxaldehyde | C6H5NO | CID 13389 - PubChem
A skin and strong eye irritant; May cause skin sensitization; [Alfa Aesar MSDS] See Pyridine-2-carbaldehyde. Search for (872-85-5[EC/RN Number]) AND (allergic OR dermatitis OR sensitizer OR sensitization): no results; [PubMed]