100719-44-6

Basic information

• Product Name: METHYL 2-METHOXYCARBONYL-3-(4-METHOXYPHENYL)-4-NITROBUTANOATE
• Synonyms: METHYL 2-METHOXYCARBONYL-3-(4-METHOXYPHENYL)-4-NITROBUTANOATE
• CAS NO: 100719-44-6
• Molecular Formula: C₁₄H₁₇NO₇
• Molecular Weight: 311.29
• Mol File: 100719-44-6.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 442.5°C at 760 mmHg
• Flash Point: 182.3°C
• Appearance: /
• Density: 1.246g/cm³
• Vapor Pressure: 5.01E-08mmHg at 25°C
• Refractive Index: 1.514
• CAS DataBase Reference: METHYL 2-METHOXYCARBONYL-3-(4-METHOXYPHENYL)-4-NITROBUTANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-METHOXYCARBONYL-3-(4-METHOXYPHENYL)-4-NITROBUTANOATE(100719-44-6)
• EPA Substance Registry System: METHYL 2-METHOXYCARBONYL-3-(4-METHOXYPHENYL)-4-NITROBUTANOATE(100719-44-6)

Safety Data

• Hazardous Substances Data: 100719-44-6(Hazardous Substances Data)

Usage

General Description

Methyl 2-methoxycarbonyl-3-(4-methoxyphenyl)-4-nitrobutanoate is a chemical compound with the molecular formula C13H17NO7. It is a nitro compound that contains a methoxy group and a carbonyl group. This chemical is commonly used as a building block in organic synthesis and pharmaceutical research. It is also used in the production of various pharmaceuticals and agrochemicals. Methyl 2-methoxycarbonyl-3-(4-methoxyphenyl)-4-nitrobutanoate is a yellow solid with a molecular weight of 295.28 g/mol and a melting point of 82-84°C.

InChI:InChI=1/C14H17NO7/c1-20-10-6-4-9(5-7-10)11(8-15(18)19)12(13(16)21-2)14(17)22-3/h4-7,11-12H,8H2,1-3H3

Upstream product

• 3179-10-0 (E)-1-methoxy-4-(2-nitrovinyl)benzene 
• 18424-76-5 sodiodimethylmalonate 
• 108-59-8 malonic acid dimethyl ester 
• 75-52-5 nitromethane 
• 123-11-5 4-methoxy-benzaldehyde 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 7443-25-6 dimethyl 2-(4-methoxybenzylidene)malonate 

Relevant articles and documents

A thiourea-functionalized metal-organic macrocycle for the catalysis of Michael additions and prominent size-selective effect

A discrete tetranuclear thiourea-based metal-organic macrocycle (MOM) with a large size was constructed by a well-designed organic ligand and nickel(ii) ions via self-assembly. Incorporating thiourea groups as hydrogen-bond donors into a metal-organic com

Urea derivative or pharmacologically acceptable salt thereof

To provide a compound having a formyl peptide receptor-like 1 (FPRL1) agonist effect. The present invention relates to a compound represented by general formula (I) or a pharmacologically acceptable salt thereof. The present invention also relates to a pharmaceutical composition which comprises the compound represented by general formula (I) or the pharmacologically acceptable salt thereof, and pharmaceutical use thereof.

An expedient and green protocol for the Michael addition of malonates, diketones and p-keto esters to the nitrostyrenes

A novel methodology has been developed for the rapid synthesis of functionalized nitroalkanes by the addition of less reactive carbon nucleophiles such as malonate esters, acetylacetone and ethyl acetoacetate to various r/ms-p-nitrostyrenes under solvent-