Welcome to LookChem.com Sign In|Join Free
  • or
(3R,4S)-ethyl 1-benzyl-4-(4-methoxyphenyl)pyrrolidine-3-carboxylate is a complex chemical compound that features an ethyl group, a benzyl group, a pyrrolidine ring, and a carboxylate group. The presence of a 4-methoxyphenyl substituent further adds to its structural intricacy. (3R,4S)-ethyl 1-benzyl-4-(4-methoxyphenyl)pyrrolidine-3-carboxylate may hold promise in pharmaceutical applications due to the inclusion of a pyrrolidine ring, which is frequently found in bioactive molecules.

2329045-02-3

Post Buying Request

2329045-02-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2329045-02-3 Usage

Uses

Used in Pharmaceutical Industry:
(3R,4S)-ethyl 1-benzyl-4-(4-methoxyphenyl)pyrrolidine-3-carboxylate is used as a potential pharmaceutical compound for its complex molecular structure that includes a pyrrolidine ring, a common feature in bioactive substances. Further research and testing are required to explore its properties and possible applications in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 2329045-02-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,3,2,9,0,4 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2329045-02:
(9*2)+(8*3)+(7*2)+(6*9)+(5*0)+(4*4)+(3*5)+(2*0)+(1*2)=143
143 % 10 = 3
So 2329045-02-3 is a valid CAS Registry Number.

2329045-02-3Downstream Products

2329045-02-3Relevant academic research and scientific papers

Electrochemical Generation of a Nonstabilized Azomethine Ylide: Access to Substituted N-Heterocycles

Kumar, Rakesh,Banerjee, Prabal

, p. 16104 - 16113 (2021/11/18)

Azomethine ylides are fascinating 1,3-dipoles for [3 + 2] cycloaddition reactions toward the construction ofN-heterocycles. Herein, an efficient and environmentally benign electrochemical approach for the generation of a nonstabilized azomethine ylide has been established under metal-free and external oxidant-free conditions. The resulting 1,3-dipole undergoes a [3 + 2] cycloaddition reaction with olefins. This electrosynthetic methodology indulges a straightforward and facile approach for the construction of substituted pyrrolidines.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2329045-02-3