1417442-89-7

Basic information

• Product Name: C₃₀H₂₃N₃O₈
• Synonyms: C₃₀H₂₃N₃O₈
• CAS NO: 1417442-89-7
• Molecular Weight: 553.528
• Mol File: 1417442-89-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₀H₂₃N₃O₈(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₂₃N₃O₈(1417442-89-7)
• EPA Substance Registry System: C₃₀H₂₃N₃O₈(1417442-89-7)

Safety Data

• Hazardous Substances Data: 1417442-89-7(Hazardous Substances Data)

Upstream product

• 136858-26-9 3-hydroxy-6-diethylamino-9-oxospiroisobenzofuran-xanthene 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 85-44-9 phthalic anhydride 
• 91-68-9 3-diethylaminophenol 
• 5809-23-4 2'-Carboxy-4-diethylamino-2-hydroxybenzophenon 

Downstream Products

• 71247-27-3 N,N-diethyl rhodol 

Relevant articles and documents

Highly selective and sensitive fluorescent sensing of N-acetylcysteine: Effective discrimination of N-acetylcysteine from cysteine

A highly selective fluorescent probe for the effective discrimination of N-acetylcysteine (NAC) from cysteine (Cys) is proposed. Probe 1 contains an N,N-diethylrhodol (DER) dye and a dinitrophenyl ether moiety. Upon mixing with NAC in aqueous cetyltrimethylammonium bromide (CTAB) micellar solution, 1 was thiolyzed by NAC to release DER, thus affording a significant increase in fluorescence emission. Whereas for Cys, it gives only a dim response at the same reaction conditions. The significant difference in reaction rates can be explained via the fact that NAC shows more hydrophobicity than Cys, therefore the Meisenheimer complex intermediate (2a) of its nucleophilic aromatic substitution with 1 can embed in CTAB micelles effectively, which will facilitate the formation of 2a and hence affords an acceleration of reaction rates. The proposed method shows an excellent selectivity for NAC over Cys, homocysteine (Hcy) and other amino acids.