59342-81-3

Basic information

• Product Name: ethyl 3-formyl-4-nitrophenyl carbonate
• CAS NO: 59342-81-3
• Molecular Formula: C₁₀H₉NO₆
• Molecular Weight: 239.1816
• Mol File: 59342-81-3.mol

Chemical Properties

• Boiling Point: 404.7°C at 760 mmHg
• Flash Point: 193.5°C
• Density: 1.379g/cm³
• Vapor Pressure: 9.25E-07mmHg at 25°C
• Refractive Index: 1.574
• CAS DataBase Reference: ethyl 3-formyl-4-nitrophenyl carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-formyl-4-nitrophenyl carbonate(59342-81-3)
• EPA Substance Registry System: ethyl 3-formyl-4-nitrophenyl carbonate(59342-81-3)

Safety Data

• Hazardous Substances Data: 59342-81-3(Hazardous Substances Data)

Upstream product

• 100-83-4 meta-hydroxybenzaldehyde 

Downstream Products

• 105728-41-4 5-(2-hydroxyethoxy)-2-nitrobenzaldehyde 
• 1255723-37-5 ethyl (2E)-2-({5-[(ethoxycarbonyl)oxy]-2-nitrophenyl}methylidene)-5-methylhex-4-enoate 
• 59342-83-5 3-carboxy-4-aminophenyl ethyl carbonate 
• 68423-37-0 2-Nitro-5-(benzyloxy)-benzylchlorid 
• 68423-36-9 (5-(benzyloxy)-2-nitrophenyl)methanol 
• 58662-54-7 5-benzyloxy-2-nitrobenzaldehyde 
• 42454-06-8 2-nitro-5-hydroxybenzaldehyde 

Relevant articles and documents

SUPRAMOLECULAR PROTEIN ASSEMBLIES WITH ADVANCED FUNCTIONS AND SYNTHESIS THEREOF

The present invention discloses stimuli-sensitive protein conjugate which can make supramolecular protein assemblies and methods for using the same. The present invention provides simple and rational process for construction of said stimuli-sensitive spherical protein assemblies through supramolecular chemical strategy.

Stable and Rapid Thiol Bioconjugation by Light-Triggered Thiomaleimide Ring Hydrolysis

Maleimide-mediated thiol-specific derivatization of biomolecules is one of the most efficacious bioconjugation approaches currently available. Alarmingly, however, recent work demonstrates that the resulting thiomaleimide conjugates are susceptible to breakdown via thiol exchange reactions. Herein, we report a new class of maleimides, namely o-CH2NHiPr phenyl maleimides, that undergo unprecedentedly rapid ring hydrolysis after thiol conjugation to form stable thiol exchange-resistant conjugates. Furthermore, we overcome the problem of low shelf lives of maleimide reagents owing to their propensity to undergo ring hydrolysis prior to bioconjugation by developing a photocaged version of this scaffold that resists ring hydrolysis. UV irradiation of thiol bioconjugates formed with this photocaged maleimide unleashes rapid thiomaleimide ring hydrolysis to yield the desired stable conjugates within 1 h under gentle, ice-cold conditions.