193264-92-5 Usage
Chemical Class
Pyrrole derivatives
Explanation
1H-Pyrrole-1,3-dicarboxylic acid, 4,5-dihydro-, 1-(1,1-dimethylethyl)
3-(phenylmethyl) ester belongs to the class of pyrrole derivatives, which are organic compounds containing a pyrrole ring.
Explanation
The compound is derived from pyrrole-1,3-dicarboxylic acid by attaching an ester group to the pyrrole ring.
3. Presence of tert-butyl and phenylmethyl groups
Explanation
The compound is characterized by the presence of both a tert-butyl (1,1-dimethylethyl) and a phenylmethyl group, which contribute to its unique chemical properties and reactivity.
Explanation
Due to its unique chemical properties and reactivity, 1H-Pyrrole-1,3-dicarboxylic acid, 4,5-dihydro-, 1-(1,1-dimethylethyl)
3-(phenylmethyl) ester is commonly used as a building block for the synthesis of various drugs and active pharmaceutical ingredients.
5. Use as a reference standard in analytical chemistry
Structure
Ester derivative of pyrrole-1,3-dicarboxylic acid
Application in pharmaceutical industry
Building block for drug synthesis
Check Digit Verification of cas no
The CAS Registry Mumber 193264-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,2,6 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193264-92:
(8*1)+(7*9)+(6*3)+(5*2)+(4*6)+(3*4)+(2*9)+(1*2)=155
155 % 10 = 5
So 193264-92-5 is a valid CAS Registry Number.
193264-92-5Relevant academic research and scientific papers
A convenient route to spiropyrrolidinyl-oxindole alkaloids via C-3 substituted ene-pyrrolidine carbamate radical cyclization
Cossy, Janine,Cases, Manuel,Gomez Pardo, Domingo
, p. 2331 - 2332 (2007/10/03)
A short access to spiropyrrolidinyl-oxindole alkaloids via a substituted ene-pyrrolidine carbamate, synthesized from the commercially available tert- butyl 1-pyrrolidine carboxylate, is described.
A convenient procedure for the conversion of N-Boc protected pyrrolidinone derivatives into their corresponding enecarbamates
Cossy,Cases,Gomez Pardo
, p. 2769 - 2776 (2007/10/03)
When N-Boc protected pyrrolidinone derivatives are treated by Dibal-H and then by quinolinium camphorsulfonate, they are converted into their corresponding enecarbamate.
