501033-98-3 Usage
Uses
Used in Organic Chemistry Research:
(Z)-2-Methoxy-5-(2-(7-Methoxy-Benzo[D][1,3]Dioxol-5-Yl)Vinyl)Aniline is used as a research compound for exploring its chemical properties and reactivity. Its unique structure allows scientists to study its interactions with other molecules and its potential use in creating new chemical entities.
Used in Drug Development:
In the pharmaceutical industry, (Z)-2-Methoxy-5-(2-(7-Methoxy-Benzo[D][1,3]Dioxol-5-Yl)Vinyl)Aniline is used as a starting material or intermediate in the synthesis of various drug candidates. Its structural features may contribute to the development of novel therapeutic agents with potential applications in treating different medical conditions.
Used in Material Science:
(Z)-2-Methoxy-5-(2-(7-Methoxy-Benzo[D][1,3]Dioxol-5-Yl)Vinyl)Aniline may also find applications in material science, particularly in the development of new polymers or other advanced materials with specific properties. Its vinyl group could be exploited in polymerization reactions to create materials with tailored characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 501033-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,3 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 501033-98:
(8*5)+(7*0)+(6*1)+(5*0)+(4*3)+(3*3)+(2*9)+(1*8)=93
93 % 10 = 3
So 501033-98-3 is a valid CAS Registry Number.
501033-98-3Relevant academic research and scientific papers
Antineoplastic agents. 487. Synthesis and biological evaluation of the antineoplastic agent 3,4-methylenedioxy-5,4′-dimethoxy-3′-amino-Z-stilbene and derived amino acid amides
Pettit, George R.,Anderson, Collin R.,Herald, Delbert L.,Katherine Jung,Lee, Debbie J.,Hamel, Ernest,Pettit, Robin K.
, p. 525 - 531 (2007/10/03)
An efficient synthesis of 3,4-methylenedioxy-5,4′-dimethoxy-3′-amino-Z-stilbene (1c) and hydrochloride (1d) is reported. The nitrostilbene intermediate 6a was obtained via a Wittig reaction using phosphonium salt 4 and 3-nitro-4-methoxybenzaldehyde 5. A o
