Welcome to LookChem.com Sign In|Join Free

CAS

  • or
TRANS-1-BOC-2-PHENYL-PYRROLIDINE-3-CARBOXYLIC ACID is a chemical compound with the molecular formula C17H23NO4, belonging to the pyrrolidine derivatives. It features a Boc (tert-butyloxycarbonyl) protecting group on the nitrogen atom, which is crucial for its stability and reactivity in chemical reactions. This white solid at room temperature is a versatile intermediate in organic synthesis and a valuable chiral building block for creating complex molecules.

870721-53-2

Post Buying Request

870721-53-2 Suppliers

Recommended suppliersmore

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

870721-53-2 Usage

Uses

Used in Pharmaceutical Industry:
TRANS-1-BOC-2-PHENYL-PYRROLIDINE-3-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and Boc protecting group make it an essential component in the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, TRANS-1-BOC-2-PHENYL-PYRROLIDINE-3-CARBOXYLIC ACID serves as a crucial intermediate for the preparation of agrochemicals. Its incorporation into the molecular structures of these compounds contributes to their effectiveness in pest control and crop protection.
Used as a Chiral Building Block:
TRANS-1-BOC-2-PHENYL-PYRROLIDINE-3-CARBOXYLIC ACID is utilized as a chiral building block in the synthesis of complex molecules. Its asymmetric center and Boc-protected nitrogen atom provide a foundation for constructing enantiomerically pure compounds, which are vital in various chemical and biological applications.
Storage and Handling:
Due to its reactivity and potential for degradation, TRANS-1-BOC-2-PHENYL-PYRROLIDINE-3-CARBOXYLIC ACID is typically handled and stored under controlled conditions. These measures ensure the preservation of its structural integrity and prevent undesired reactions, maintaining its utility in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 870721-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,7,2 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 870721-53:
(8*8)+(7*7)+(6*0)+(5*7)+(4*2)+(3*1)+(2*5)+(1*3)=172
172 % 10 = 2
So 870721-53-2 is a valid CAS Registry Number.

870721-53-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-1-[(2-methylpropan-2-yl)oxycarbonyl]-2-phenylpyrrolidine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,3-Pyrrolidinedicarboxylicacid,2-phenyl-,1-(1,1-dimethylethyl) ester,(2R,3R)-rel

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:870721-53-2 SDS

870721-53-2Downstream Products

870721-53-2Relevant articles and documents

SUBSTITUTED PYRROLIDINE AMIDES V

-

, (2021/01/22)

The invention relates to compounds according to general formula (I), which act as modulators of the glucocorticoid receptor and can be used in the treatment and/or prophylaxis of disorders which are at least partially mediated by the glucocorticoid receptor.

Diastereoselective access to enantiomerically pure cis-2,3-disubstituted pyrrolidines

Delaye, Pierre-Olivier,Pradhan, Tanin K.,Lambert, Emilie,Vasse, Jean-Luc,Szymoniak, Jan

experimental part, p. 3395 - 3406 (2010/08/20)

A straightforward access to enantiomerically pure 2,3-disubstituted pyrrolidines is reported that involves diastereoselective allylation of (R)-phenylglycinol-derived imines and a sequential hydrozirconation-cyclization. A number of pyrrolidine derivatives bearing aryl, heteroaryl, alkyl and alkenyl groups have been prepared in this way. Such compounds are useful building blocks in the synthesis of molecules of biological interest, as illustrated by the syntheses of proline derivatives and the naturally occurring alkaloid (-)-isoretronecanol.

3-AMINO-2-PHENYLPYRROLIDINE DERIVATIVES

-

Page/Page column 78, (2010/02/14)

3-amino-2-phenylpyrrolidine compounds useful as NK-1 antagonists, with pharmaceutical compositions and methods of treatment comprising same, are disclosed.

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

What can I do for you?
Get Best Price

Get Best Price for 870721-53-2