55125-78-5

Basic information

• Product Name: carbon monoxide
• Synonyms: carbon monoxide
• CAS NO: 55125-78-5
• Molecular Weight: 30.011
• Mol File: 55125-78-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: carbon monoxide(CAS DataBase Reference)
• NIST Chemistry Reference: carbon monoxide(55125-78-5)
• EPA Substance Registry System: carbon monoxide(55125-78-5)

Safety Data

• Hazardous Substances Data: 55125-78-5(Hazardous Substances Data)

Upstream product

• 51060-05-0 fulminic acid 
• 1632-99-1 ethane-d6 
• 15917-79-0 H₂⁽¹⁵⁾N⁽¹⁸⁾O 
• 32767-18-3 oxygen-18 
• 201230-82-2 carbon monoxide 
• 7732-18-5 water 
• 14797-71-8 ¹⁸O-labeled water 
• 67-56-1 methanol 
• 1397685-14-1 1-(9-(1,3-dithian-2-yl)-6-(piperidin-1-yl)-3H-xanthen-3-ylidene)piperidin-1-ium chloride 
• 78921-00-3 dichloro-deuterio-iodo-methane 
• 594-04-7 dichloroiodomethane 
• 14742-23-5 ethanol-1-13C 
• 107-02-8 acrolein 
• 41061-01-2 bis(2,2'-bipyridyl)(carbonyl)chlororuthenium(II) chloride 

Downstream Products

• 34979-99-2 uranium monoxide 
• 124-38-9 carbon dioxide 
• 2537-69-1 carbon dioxide 
• 18983-82-9 CO⁽¹⁸⁾O 
• 889868-85-3 Ni(CO)3(C⁽¹⁸⁾O) 
• 201230-82-2 carbon monoxide 

Relevant articles and documents

IR spectroscopic study of the dichloromethyl peroxyl radical and its deuterated analogs in the argon matrix

The dichloromethyl peroxyl radical (CHCl2OO?) and its deuterated analog formed in the reaction of the corresponding dichloromethyl radicals with O2 were studied by matrix IR spectroscopy. Dichloromethyl radicals are genera

Direct Synthesis of 2-Formylpyrrolidines, 2-Pyrrolidinones and 2-Dihydrofuranones via Aerobic Copper-Catalyzed Aminooxygenation and Dioxygenation of 4-Pentenylsulfonamides and 4-Pentenylalcohols

A new method for the direct conversion of 4-pentenylsulfonamides to 2-formylpyrrolidines and a 2-ketopyrrolidine has been developed. This transformation occurs via aerobic copper-catalyzed alkene aminooxygenation where molecular oxygen serves as both oxidant and oxygen source. The 2-formylpyrrolidines can further undergo oxidative carbon-carbon bond cleavage in situ upon addition of DABCO, providing 2-pyrrolidinones. These transformations have been demonstrated for a range of 4-pentenylsulfonamides. 4-Pentenylalcohols also undergo oxidative cyclization to form γ-lactones predominantly. The reaction is chemoselective, oxidizing one alkene in the presence of others, and is compatible with several functional groups. Application of these reactions to the formal syntheses of baclofen and (+)-monomorine was demonstrated.

Pd/K/Co-oxide catalyst for water gas shift

Various Co3O4 catalysts were investigated for the water gas shift (WGS) reaction for hydrogen production. Although the catalyst supporting only palladium (Pd/Co3O4) showed low catalytic activity and higher selec