17490-72-1

Basic information

• Product Name: 2-[(4-NITROBENZYL)OXY]BENZALDEHYDE
• Synonyms: TIMTEC-BB SBB001482;CHEMBRDG-BB 5566707;ASISCHEM N43069;2-[(4-NITROBENZYL)OXY]BENZALDEHYDE;OTAVA-BB 7020673534;benzaldehyde, 2-[(4-nitrophenyl)methoxy]-;2-[(4-nitrobenzyl)oxy]benzaldehyde(SALTDATA: FREE)
• CAS NO: 17490-72-1
• Molecular Formula: C₁₄H₁₁NO₄
• Molecular Weight: 257.24
• Mol File: 17490-72-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 451°C at 760 mmHg
• Flash Point: 207.5°C
• Appearance: /
• Density: 1.301g/cm³
• Vapor Pressure: 2.52E-08mmHg at 25°C
• Refractive Index: 1.634
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-[(4-NITROBENZYL)OXY]BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-NITROBENZYL)OXY]BENZALDEHYDE(17490-72-1)
• EPA Substance Registry System: 2-[(4-NITROBENZYL)OXY]BENZALDEHYDE(17490-72-1)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 17490-72-1(Hazardous Substances Data)

Usage

General Description

2-[(4-Nitrobenzyl)oxy]benzaldehyde is a chemical compound with the molecular formula C14H11NO4. It is a benzaldehyde derivative with a nitro group and a benzyl ether functional group. 2-[(4-NITROBENZYL)OXY]BENZALDEHYDE is used in the synthesis of various pharmaceuticals and organic compounds. It has potential applications in the fields of medicine, agriculture, and materials science. The presence of the nitro group makes it a valuable component for chemical reactions and organic synthesis processes. It is important to handle this compound with caution due to its potential hazards and toxic effects.

InChI:InChI=1/C14H11NO4/c16-9-12-3-1-2-4-14(12)19-10-11-5-7-13(8-6-11)15(17)18/h1-9H,10H2

Upstream product

• 90-02-8 salicylaldehyde 
• 100-11-8 1-bromomethyl-4-nitro-benzene 

Downstream Products

• 787-64-4 2-(4-nitrophenyl)-1-benzofurane 
• 1416064-80-6 C₃₂H₄₀N₄O₅ 
• 101046-17-7 N-<4-(2-benzofuranyl)phenyl>maleamic acid 
• 782-18-3 4-(benzofuran-2-yl)benzenamine 

Relevant articles and documents

Inhibition of Ebola virus infection: Identification of niemann-pick C1 as the target by optimization of a chemical probe

A high-throughput screen identified adamantane dipeptide 1 as an inhibitor of Ebola virus (EboV) infection. Hit-to-lead optimization to determine the structure-activity relationship (SAR) identified the more potent EboV inhibitor 2 and a photoaffinity labeling agent 3. These antiviral compounds were employed to identify the target as Niemann-Pick C1 (NPC1), a host protein that binds the EboV glycoprotein and is essential for infection. These studies establish NPC1 as a promising target for antiviral therapy.

Development and Application of Organic Reagents for Analysis. VI. Synthesis and Fluorescence Spectral Properties of 2-(4-Substituted phenyl)benzofurans

A synthesis of fifteen kinds of 2-(4-substituted phenyl)benzofurans (4n) was carried out and their fluorescence spectral properties were investigated concerning their applicability as organic reagents for analyses.