146060-06-2

Basic information

• Product Name: copper(I) oxide
• CAS NO: 146060-06-2
• Molecular Weight: 143.091
• Mol File: 146060-06-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: copper(I) oxide(CAS DataBase Reference)
• NIST Chemistry Reference: copper(I) oxide(146060-06-2)
• EPA Substance Registry System: copper(I) oxide(146060-06-2)

Safety Data

• Hazardous Substances Data: 146060-06-2(Hazardous Substances Data)

Upstream product

• 12775-96-1 copper 

Downstream Products

• 15288-01-4 7-hydroxy-6-methoxy-3,4-dihydronaphthalen-1(2H)-one 
• 223133-18-4 2-chloro-3,5-dimethylbenzene-1,4-diol 
• 149556-23-0 N-cyclohexyl-4-(3,5-dimethoxyphenoxy)-N-(1-methylethyl)benzamide 
• 140157-68-2 ethyl alpha-bromo-4-[ 2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzenepropanoate 
• 149556-17-2 N-cyclohexyl-4-(3,4-dimethoxyphenoxy)-N-(1-methylethyl)benzamide 
• 149556-16-1 N-cyclohexyl-N-cyclopentyl-4-(3,4-dimethoxyphenoxy)benzamide 
• 149556-18-3 N,N-dicyclopentyl-4-(3,4-dimethoxyphenoxy)benzamide 
• 149556-12-7 N-cyclohexyl-N-(1-methylethyl)-4-(3,4,5-trimethoxyphenoxy)benzamide 
• 149556-15-0 N-cyclohexyl-N-cyclopentyl-4-(3,4,5-trimethoxyphenoxy)benzamide 
• 149556-30-9 N-cyclohexyl-3-methoxy-N-(1-methylethyl)-4-(3,4,5-trimethoxyphenoxy)benzamide 
• 1243969-29-0 N-cyclohexyl-N-(n-hexyl)-4-(3,4,5-trimethoxyphenoxy)benzamide 
• 1243969-23-4 N-cyclohexyl-3-ethoxy-N-(1-methylethyl)-4-(3,4,5-trimethoxyphenoxy)benzamid 
• 1243969-26-7 3-chloro-N-cyclohexyl-N-(1-methylethyl)-4-(3,4,5-trimethoxyphenoxy)benzamide 
• 69747-21-3 ethyl 4-hydroxy-3-methylbenzoate 

Relevant articles and documents

Oxidation of Copper in Nitrogen Dioxide

Thermal microgravimetry, mass spectrometry, and X-ray diffractometry were used to investigate the ability of NO2 to oxidize copper.NO2 oxidizes a copper plate with formation of oxide film consisting of Cu2O (predominant) and CuO.The oxidation obeys a cubic law, and proceeds faster than in oxygen.An oxidation mechanism is presented on the basis of kinetic and structural data.

Microbicidal N-sulfonylglycin alkynyloxyphenethyl amide derivatives

The invention relates to novel pesticidally active compounds of the general formula I as well as possible isomers and mixtures of isomers thereof, wherein n is a number zero or one; and R1is C1-C12alkyl that is unsubstituted or may be substituted by C1-C4alkoxy, C1-C4alkylthio, C1-C4alkylsulfonyl, C3-C8cycloalkyl, cyano, C1C6alkoxycarbonyl, C3-C6alkenyloxycarbonyl or by C3-C6alkynyloxycarbonyl; C3-C8cycloalkyl; C2-C12alkenyl; C2-C12alkynyl; C1-C12haloalkyl: or a group NR11R12wherein R11and R12are each independently of the other hydrogen or C1-C8alkyl, or together are tetra- or penta-methylene; R2and R3are each independently of the other hydrogen; C1-C8alkyl; C1-C8alkyl substituted by hydroxy, C1-C4alkoxy, mercapto or by C1-C4alkylthio; C3-C8alkenyl; C3-C8alkynyl; C3-C8cycloalkyl; C3-C8cycloalkyl-C1-C4alkyl; or the two groups R2and R3together with the carbon atom to which they are bonded form a three- to eight-membered ring; R4, R5, R6and R7are identical or different and are each independently of the others hydrogen or C1-C4alkyl; R8is C1-C6alkyl, C3-C6alkenyl or C3-C6alkynyl; A is C1-C6alkylene; and B is optionally mono- or poly-nuclear, unsubstituted or substituted aryl; optionally mono- or poly-nuclear, unsubstituted or substituted heteroaryl; C4-C12alkyl; or C3-C8cycloalkyl. The novel compounds have plant-protecting properties and are suitable for protecting plants against infestation by phytopathogenic microorganisms.