29865-49-4

Basic information

• Product Name: (4-METHOXYPHENYL)-2-NITROPROPANE
• Synonyms: 1-(4-METHOXYPHENYL)-2-NITROPROPANE;(4-METHOXYPHENYL)-2-NITROPROPANE
• CAS NO: 29865-49-4
• Molecular Formula: C₁₀H₁₃NO₃
• Molecular Weight: 195.22
• Mol File: 29865-49-4.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 313.5 °C at 760 mmHg
• Flash Point: 139.2 °C
• Appearance: /
• Density: 1.109 g/cm³
• CAS DataBase Reference: (4-METHOXYPHENYL)-2-NITROPROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: (4-METHOXYPHENYL)-2-NITROPROPANE(29865-49-4)
• EPA Substance Registry System: (4-METHOXYPHENYL)-2-NITROPROPANE(29865-49-4)

Safety Data

• Hazardous Substances Data: 29865-49-4(Hazardous Substances Data)

Usage

General Description

(4-METHOXYPHENYL)-2-NITROPROPANE is a chemical compound with the molecular formula C10H13NO3. It is a yellow crystalline solid that is used in the synthesis of various pharmaceutical and agrochemical products. (4-METHOXYPHENYL)-2-NITROPROPANE is a nitroalkene derivative, and its structure consists of a nitro group attached to a propyl chain with a 4-methoxyphenyl group. (4-METHOXYPHENYL)-2-NITROPROPANE is primarily used as an intermediate in the production of other chemicals and is not widely used in commercial applications. It is important to handle this compound with care due to its potential hazardous properties.

Upstream product

• 17354-63-1 4-(2-nitro-propenyl)-anisole 
• 31236-71-2 lysichitalexin 
• 74-88-4 methyl iodide 
• 123-11-5 4-methoxy-benzaldehyde 
• 148527-33-7 2-nitro-1-hydroxy-1-(4-methoxy-phenyl)-propane 
• 148527-35-9 1-(4-methoxyphenyl)-2-nitropropyl acetate 
• 79-24-3 Nitroethane 
• 105-13-5 4-Methoxybenzyl alcohol 
• 37629-51-9 1-methoxy-4-((E)-2-nitroprop-1-enyl)benzene 

Downstream Products

• 122-84-9 4-methoxybenzyl methyl ketone 
• 36176-47-3 1-(hydroxyimino-(seqtrans))-1-(4-methoxy-phenyl)-acetone 
• 874-90-8 4-methoxybenzonitrile 
• 86886-42-2 N-(1-hydroxy-3-(4-methoxyphenyl)propan-2-yl)acetamide 

Relevant articles and documents

Sequential Acylation/Silylation/Hetero-Claisen Rearrangement of Nitroalkanes for the Synthesis of Protected Hydroxyoxime Derivatives

Sequential acylation-silylation of nitroalkanes leads to O-silylated α-acyloxyoximes in high yields. The first step of the reaction involves deprotonation of nitro compound with sodium hydride promoted by DBU or alcohol/15-crown-5 system followed by treat

Nickel-Catalyzed C-Alkylation of Nitroalkanes with Unactivated Alkyl Iodides

Enabled by nickel catalysis, a mild and general catalytic method for C-alkylation of nitroalkanes with unactivated alkyl iodides is described. Compatible with primary, secondary, and tertiary alkyl iodides; and tolerant of a wide range of functional groups, this method allows rapid access to diverse nitroalkanes.

The highly chemoselective transfer hydrogenation of the carbon-carbon double bond of conjugated nitroalkenes by a rhodium complex

Chemoselective transfer hydrogenation of conjugated nitroalkenes catalyzed by [RhCl2Cp·]2-diamine complex (Cp ·=η5-C5Me5) using HCOOH/Et3N (5:2) (TEAF) as a hydrogen source was realized. A variety of nitrostyrenes, β-methyl nitrostyrenes, and 3-methyl-4-nitro-5-alkenyl- isoxazoles were reduced smoothly in good to excellent yields in short reaction time. Other functional groups are inert under the reaction conditions.