127865-40-1

Basic information

• Product Name: Benzene, 1-methoxy-4-[2-nitro-1-(2-propenylthio)ethyl]-
• CAS NO: 127865-40-1
• Molecular Formula: C12H15NO3S
• Molecular Weight: 253.322
• Mol File: 127865-40-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1-methoxy-4-[2-nitro-1-(2-propenylthio)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methoxy-4-[2-nitro-1-(2-propenylthio)ethyl]-(127865-40-1)
• EPA Substance Registry System: Benzene, 1-methoxy-4-[2-nitro-1-(2-propenylthio)ethyl]-(127865-40-1)

Safety Data

• Hazardous Substances Data: 127865-40-1(Hazardous Substances Data)

Upstream product

• 870-23-5 prop-2-ene-1-thiol 
• 3179-10-0 (E)-1-methoxy-4-(2-nitrovinyl)benzene 
• 75-52-5 nitromethane 
• 123-11-5 4-methoxy-benzaldehyde 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 

Downstream Products

• 127865-51-4 6-(4-methoxyphenyl)-3,3a,4,6-tetrahydrothiopheno<3,4-c>isoxazole 
• 127865-46-7 6-(4-methoxyphenyl)-3,3a,4,6-tetrahydrothiopheno<3,4-c>isoxazole 
• 128869-59-0 cis-3-amino-4-(hydroxymethyl)-trans-2-(4-methoxyphenyl)tetrahydrothiophene 
• 128869-60-3 3-(hydroxymethyl)-1-(4-methoxyphenyl)-2-butanone 

Relevant articles and documents

A theoretical evaluation of the Michael-acceptor ability of conjugated nitroalkenes

A theoretical evaluation of the relative Michael-acceptor abilities of a variety of substituted aromatic and aliphatic nitroalkenes is reported. Several global and local reactivity indices were evaluated with the incorporation of natural charge obtained f

Pesticidal and parasiticidal use of 1-aryl-1-(substituted thio, sulfinyl and sulfonyl)-2-nitroethane compounds

The present invention relates to the pesticidal use of 1-aryl-1-(substituted thio, sulfinyl and sulfonyl)-2-nitroethane compounds having the structural formula I

A Two-Step Conversion of Carbonyl Compounds into Functionalized Five- and Six-Membered Ring Thioethers via Intramolecular Cycloaddition

Reaction of aldehydes or ketones with nitromethane in the presence of unsaturated thiols led directly to unsaturated nitro sulfides 7, 12, 14, or 19.These compounds were converted by intramolecular nitrile oxide-olefin cycloaddition to tetrahydrothiopheno