155988-38-8

Basic information

• Product Name: 1-(2-NITROPHENYL)-2-NITROPROPENE
• Synonyms: 1-(2-NITROPHENYL)-2-NITROPROPENE
• CAS NO: 155988-38-8
• Molecular Formula: C9H8N2O4
• Molecular Weight: 208.17
• Mol File: 155988-38-8.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 356.7°C at 760 mmHg
• Flash Point: 176.5°C
• Appearance: /
• Density: 1.344g/cm³
• Vapor Pressure: 5.91E-05mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: 1-(2-NITROPHENYL)-2-NITROPROPENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-NITROPHENYL)-2-NITROPROPENE(155988-38-8)
• EPA Substance Registry System: 1-(2-NITROPHENYL)-2-NITROPROPENE(155988-38-8)

Safety Data

• Hazardous Substances Data: 155988-38-8(Hazardous Substances Data)

Usage

General Description

1-(2-NITROPHENYL)-2-NITROPROPENE is a chemical compound with the molecular formula C9H7NO4. It is a nitroalkene, which means it contains a nitro group and a carbon-carbon double bond. 1-(2-NITROPHENYL)-2-NITROPROPENE is commonly used in organic synthesis and as a building block for the preparation of various other chemical compounds. It is known for its potential as a precursor in the synthesis of pharmaceuticals and agrochemicals. Additionally, it has been studied for its potential use in the development of new materials and as a reagent in organic reactions. However, it is important to handle this compound with caution due to its potential hazards and toxicity.

InChI:InChI=1/C9H8N2O4/c1-7(10(12)13)6-8-4-2-3-5-9(8)11(14)15/h2-6H,1H3/b7-6+

Upstream product

• 552-89-6 2-nitro-benzaldehyde 
• 79-24-3 Nitroethane 
• 14841-89-5 1-(2-nitrophenyl)-2-nitropropan-1-ol 

Downstream Products

• 1426682-60-1 2-methyl-3-(2-nitrophenyl)quinoxaline 
• 921-11-9 2,3,4-pentanetrione 
• 109704-02-1 Methyl<2,5-dimethyl-4-(2-nitrophenyl)-3-pyrrolyl>keton 
• 86396-16-9 methyl 2,3-dioxobutanoate 
• 95838-57-6 2,5-Dimethyl-4-(2-nitrophenyl)-3-pyrrolcarbonsaeure-methylester 

Relevant articles and documents

Synthesis of novel 3-halo-3-nitroflavanones and their activities as DNA methyltransferase inhibitors in cancer cells

The implication of DNA methylation in cancer is today clearly established. Despite that nucleoside analogues are currently used for leukaemia treatment, their low stability in physiological conditions and their lack of selectivity arise the need for the i

Convenient modification of the Leimgruber-Batcho indole synthesis: Reduction of 2-nitro-p-pyrrolidinostyrenes by the FeCl3-activated carbon-N2H4H2O system

A new catalytic system containing ferric chloride, activated carbon, and hydrazine has been proposed for the reductive cyclization of β-dialkylamino-2-nitrostyrenes to give the corresponding indoles (Leimgruber-Batcho synthesis). Various substituted indoles may be obtained in high yield under these conditions.

A general large scale synthesis of 2-alkyl-7-methoxyindoles

A general method has been developed for the large scale synthesis of 2-alkyl-7-methoxyindoles and analogs. This method involves an efficient preparation of the key intermediates, 1-(2-nitroaryl)-2-nitroalkanols and 1-(2-nitroaryl)-2-nitroalkenes, and affords 2-alkyl-7-methoxyindoles and analogs in 3 steps with good overall yields.