104655-33-6 Usage
Type of compound
Ester derivative
Parent compound
1-amino-2-hydroxy-naphtalene-3-carboxylic acid
Common uses
Synthesis of pharmaceuticals and other organic compounds
Potential applications
Building block for creating more complex molecules
Safety concerns
Potential hazards associated with use and handling
Structure
Unique structure that contributes to its properties and applications
Chemical properties
May vary depending on the specific reaction conditions and other factors
Physical properties
May include appearance, solubility, melting point, and boiling point
Stability
May be sensitive to certain conditions such as light, heat, or moisture
Reactivity
May react with other chemicals, potentially leading to hazardous situations
Storage
Should be stored in a cool, dry place, away from incompatible substances
Disposal
Should be disposed of according to local regulations and safety guidelines
Regulatory status
May be subject to certain regulations depending on the country or region
Environmental impact
Potential environmental impact if not handled and disposed of properly.
Check Digit Verification of cas no
The CAS Registry Mumber 104655-33-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,5 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104655-33:
(8*1)+(7*0)+(6*4)+(5*6)+(4*5)+(3*5)+(2*3)+(1*3)=106
106 % 10 = 6
So 104655-33-6 is a valid CAS Registry Number.
104655-33-6Relevant articles and documents
Synthesis and evaluation of an O-Aminated naphthol AS-E as a prodrug of CREB-mediated gene transcription inhibition
Xie, Fuchun,Li, Bingbing X.,Xiao, Xiangshu
, p. 380 - 384 (2013/07/26)
An O-Aminated naphthol AS-E was designed as a prodrug to achieve reductive activation and improved aqueous solubility. During the synthesis of this designed compound, a novel transformation from aryl triflates and ethyl acetohydroximate to oxazoles was discovered. Although the initially designed O-Amino naphthol AS-E was not made successfully, the eventually synthesized O-tert-butylamino derivative was found to be biologically inactive, suggesting that reductive N-O cleavage in this compound was not facile due to unfavorable steric and electronic effects.
