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(2R)-N-Methyl-2-PyrrolidinecarboxaMide is a chemical compound with the molecular formula C6H12N2O. It is a derivative of pyrrolidine and has potential uses in pharmaceutical research. (2R)-N-Methyl-2-PyrrolidinecarboxaMide is notable for its ability to penetrate the blood-brain barrier, which makes it a promising candidate for drug delivery to the central nervous system (CNS). Its unique structure and properties also position it as a potential building block for the synthesis of other pharmaceutical compounds, contributing to its interest for further research and development in the pharmaceutical industry.

66877-05-2

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66877-05-2 Usage

Uses

Used in Pharmaceutical Research:
(2R)-N-Methyl-2-PyrrolidinecarboxaMide is used as a research compound for the development of new pharmaceuticals, particularly those targeting the central nervous system. Its ability to cross the blood-brain barrier is a significant advantage for the treatment of CNS disorders and neurological diseases.
Used in Drug Delivery to the Central Nervous System:
As a potential drug delivery candidate, (2R)-N-Methyl-2-PyrrolidinecarboxaMide is used for facilitating the transport of therapeutic agents to the CNS. This application is crucial for the treatment of various neurological conditions that require precise targeting and effective drug concentrations within the brain.
Used as a Building Block for Pharmaceutical Synthesis:
(2R)-N-Methyl-2-PyrrolidinecarboxaMide also serves as a key component in the synthesis of other pharmaceutical compounds. Its unique structural features make it a valuable asset in the creation of new drugs with specific therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 66877-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66877-05:
(7*6)+(6*6)+(5*8)+(4*7)+(3*7)+(2*0)+(1*5)=172
172 % 10 = 2
So 66877-05-2 is a valid CAS Registry Number.

66877-05-2SDS

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 (R)-proline methylamide

1.2 Other means of identification

Product number -
Other names (R)-N-Methyl-2-pyrrolidinecarboxamide HCl

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:66877-05-2 SDS

66877-05-2Downstream Products

66877-05-2Relevant academic research and scientific papers

QUINAZOLINEDIONE DERIVATIVE

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Paragraph 1660; 1662, (2015/03/16)

The present invention relates to quinazolinedione derivatives represented by formula (I) or pharmaceutically acceptable salts thereof.

Synthesis, characterisation and in vitro cytotoxicity studies of a series of chiral platinum(II) complexes based on the 2-aminomethylpyrrolidine ligand: X-ray crystal structure of [PtCl2(R-dimepyrr)] (R-dimepyrr = N-dimethyl-2(R)-aminomethylpyrrolidine)

Diakos, Connie I.,Zhang, Mei,Beale, Philip J.,Fenton, Ronald R.,Hambley, Trevor W.

experimental part, p. 2807 - 2814 (2009/10/10)

A series of platinum(II) complexes were synthesised based on the enantiomerically pure amino acid proline. Novel synthetic pathways were developed, adapted from standard peptide chemistry, to produce the 2-aminomethylpyrrolidine (pyrr) ligand and its derivatives with differing arrangements of methyl substituents at the exocyclic amine sites. The crystal structure of [PtCl2(R-dimepyrr)] (R-dimepyrr = N,N-dimethyl-2(R)-aminomethylpyrrolidine) is reported and the five-membered ligand ring has been shown to be in an envelope conformation. Cytotoxicity studies were carried out on the ovarian cancer A2780 tumour cell line and its cisplatin-resistant variant, A2780cisR. Remarkably good activity was seen for several of the drugs when compared to cisplatin despite the addition of substantial steric bulk to the amine groups, and there was a lack of cross-resistance with cisplatin seen for some compounds.

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