295344-96-6 Usage
Uses
Used in Pharmaceutical Industry:
3-(4-Methoxy-phenyl)-3-(toluene-4-sulfonylamino)-propionic acid is used as a pharmaceutical intermediate for the synthesis of various organic compounds. Its unique structural properties make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Chemical Industry:
In the chemical industry, 3-(4-Methoxy-phenyl)-3-(toluene-4-sulfonylamino)-propionic acid is utilized in the synthesis of a wide range of organic compounds. Its versatile structure allows for its use in various chemical reactions, contributing to the development of new chemical products and materials.
Used in Research and Development:
3-(4-Methoxy-phenyl)-3-(toluene-4-sulfonylamino)-propionic acid is employed in research and development for its potential therapeutic applications. Its unique structural properties make it an interesting compound for scientists to study and explore its potential uses in the pharmaceutical field. 3-(4-METHOXY-PHENYL)-3-(TOLUENE-4-SULFONYLAMINO)-PROPIONIC ACID can be further modified or combined with other molecules to create new drugs or improve existing ones, contributing to the advancement of medical treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 295344-96-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,5,3,4 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 295344-96:
(8*2)+(7*9)+(6*5)+(5*3)+(4*4)+(3*4)+(2*9)+(1*6)=176
176 % 10 = 6
So 295344-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H19NO5S/c1-12-3-9-15(10-4-12)24(21,22)18-16(11-17(19)20)13-5-7-14(23-2)8-6-13/h3-10,16,18H,11H2,1-2H3,(H,19,20)/p-1/t16-/m1/s1
295344-96-6Relevant academic research and scientific papers
Stereoselective synthesis of activated 2-arylazetidines via imino-aldol reaction
Ghorai, Manas K.,Das, Subhomoy,Das, Kalpataru,Kumar, Amit
, p. 9042 - 9049 (2015/09/01)
A simple and efficient synthetic route to substituted N-sulfinyl and N-sulfonyl azetidines is described involving imino-aldol reaction of ester enolates with racemic and non-racemic aldimines for obtaining β-amino esters as a key step. These β-amino ester
