6283-12-1

Basic information

• Product Name: 2-(4-methoxyphenyl)-5-methyl-5-nitro-1,3-dioxane
• CAS NO: 6283-12-1
• Molecular Formula: C₁₂H₁₅NO₅
• Molecular Weight: 253.2512
• Mol File: 6283-12-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 390.7°C at 760 mmHg
• Flash Point: 172.7°C
• Density: 1.25g/cm³
• Vapor Pressure: 2.61E-06mmHg at 25°C
• Refractive Index: 1.545
• CAS DataBase Reference: 2-(4-methoxyphenyl)-5-methyl-5-nitro-1,3-dioxane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxyphenyl)-5-methyl-5-nitro-1,3-dioxane(6283-12-1)
• EPA Substance Registry System: 2-(4-methoxyphenyl)-5-methyl-5-nitro-1,3-dioxane(6283-12-1)

Safety Data

• Hazardous Substances Data: 6283-12-1(Hazardous Substances Data)

Usage

Nitroalkane derivative

It is a derivative of nitroalkanes A class of organic compounds containing a nitro group (-NO2) attached to an alkane carbon chain.

Dioxane ring

A six-membered cyclic ether structure The compound contains a 1,3-dioxane ring, which is a six-membered ring with two oxygen atoms connected by carbon atoms.

Methoxyphenyl group

Presence of a phenyl group with a methoxy substituent (-OCH3) A phenyl group (a benzene ring) is attached to the dioxane ring, and it has a methoxy group as a substituent, enhancing its reactivity and biological activity.

Organic synthesis and pharmaceutical research

Widely used in these fields The compound is commonly used in organic synthesis and pharmaceutical research due to its unique chemical properties.

Antimicrobial and antifungal activities

Potential applications in fighting infections The compound is known for its potential to exhibit antimicrobial and antifungal properties, making it a valuable compound in various scientific applications.

Reactivity and biological activity

Influenced by methyl and nitro groups The presence of a methyl group (-CH3) and a nitro group (-NO2) in the molecule contribute to its reactivity and biological activity, making it a valuable compound in scientific research and applications.

Upstream product

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Relevant articles and documents

Catalytically Enantioselective Synthesis of Acyclic α-Tertiary Amines through Desymmetrization of 2-Substituted 2-Nitro-1,3-diols

Highly enantioselective synthesis of acyclic α-tertiary amines through asymmetric desymmetrization is reported. This approach is based on chiral phosphoric acid mediated, enantioselective, oxidative desymmetrization of 2-substituted 2-nitro-1,3-diolbenzylidine acetals in the presence of DMDO as an oxidant. The method allows for the formation of a wide variety of chiral 2-nitro-1,3-diols in high enantioselectivity, which could be transformed into optically pure, unnatural α-alkyl series. The synthetic utility of this method has been further demonstrated by the expedient construction of the core structure of natural products manzacidins enantioselectively.