15121-85-4

Basic information

• Product Name: 1,3-Propanediol, 2-(2-nitrophenyl)-
• CAS NO: 15121-85-4
• Molecular Formula: C9H11NO4
• Molecular Weight: 197.191
• Mol File: 15121-85-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 404.3±30.0 °C(Predicted)
• Density: 1.347±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,3-Propanediol, 2-(2-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Propanediol, 2-(2-nitrophenyl)-(15121-85-4)
• EPA Substance Registry System: 1,3-Propanediol, 2-(2-nitrophenyl)-(15121-85-4)

Safety Data

• Hazardous Substances Data: 15121-85-4(Hazardous Substances Data)

Upstream product

• 26465-37-2 dimethyl 2-(2-nitrophenyl)malonate 
• 50-00-0 formaldehyd 
• 88-72-2 1-methyl-2-nitrobenzene 

Downstream Products

• 130469-60-2 1-(tert-Butyloxycarbonyl)-3-(methanesulfonyloxymethyl)indoline 
• 127843-10-1 2,3-epoxy-2-(2-nitrophenyl)propionaldehyde 
• 1504-06-9 3-methylindolin-2-one 
• 83-34-1 3-Methylindole 
• 118481-30-4 1-(methanesulfonyl)-1H-indole-3-carboxaldehyde 
• 115444-91-2 methanesulfonic acid 3-methanesulfonyloxy-2-(2-nitrophenyl)-propyl ester 
• 54892-85-2 2-(2-aminophenyl)-1,3-propanediol 
• 71463-16-6 2-(2-nitrophenyl)propenal 
• 552-16-9 ortho-nitrobenzoic acid 
• 155088-50-9 3-Nitro-4-(2-nitro-phenyl)-4,5-dihydro-isoxazole 

Relevant articles and documents

Probing cytochrome P450 (CYP) bioactivation with chloromethylindoline bioprecursors derived from the duocarmycin family of compounds

The duocarmycins belong to a class of agent which has great potential for use in cancer therapy. Their exquisite potency means they are too toxic for systemic use, and targeted approaches are required to unlock their clinical potential. In this study, we

A chemoselective photolabile protecting group for aldehydes

A new and high-efficiency photolabile protecting group (PLPG) for aldehydes is described. The PLPG was introduced to aldehydes by using a Lewis acid. Results showed that the PLPG can be released rapidly and smoothly under ultraviolet (UV) irradiation with high efficiency and low cost. This PLPG can easily synthesized and also be selectively protect aldehydes in the presence of ketones.

Electrogenerated Base (EG Base) Induced Hydroxymethylation of the Side Chain of Nitroalkylbenzenes with Paraformaldehyde

Hydroxymethylation of nitroalkylbenzenes with paraformaldehyde was accomplished by electrolysis in a (CH2O)n-DMF-Et4NOTs-(Pt electrode) system.The reaction was found to be catalytic (0.25 faraday/mol) and dependent on the electroreduction of formaldehyde and/or nitroalkylbenzene.A variety of nitroalkylbenzenes were transformed to their corresponding mono- and/or bishydroxymethylated derivatives in good yield.The product yield and selectivity were shown to depend on the order of reagent addition, solvent, supporting electrolyte, and structure of the starting nitroalkylbenzenes.A plausible mechanism of the generation of base catalysts (EG base) in electroreductive media is discussed.