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5731-17-9

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5731-17-9 Usage

Description

1-BENZYLPYRROLIDIN-3-YL-METHANOL is a chemical compound characterized by the molecular formula C14H19NO. It is a derivative of pyrrolidinomethanols, which are recognized for their potential pharmacological properties. 1-BENZYLPYRROLIDIN-3-YL-METHANOL features a benzyl group attached to the pyrrolidin-3-yl-methanol moiety, making it a significant building block in the synthesis of various pharmaceuticals and bioactive compounds. Its unique structure and properties render it a valuable asset in medicinal chemistry and chemical biology for the discovery of new drugs for diverse therapeutic applications.

Uses

Used in Pharmaceutical Research and Development:
1-BENZYLPYRROLIDIN-3-YL-METHANOL is used as a key building block for the synthesis of pharmaceuticals and bioactive compounds. Its presence in the molecular structure of these compounds contributes to their potential therapeutic effects.
Used in Medicinal Chemistry:
1-BENZYLPYRROLIDIN-3-YL-METHANOL is utilized as a valuable tool in medicinal chemistry for the exploration of new drug candidates. Its unique structure allows for the development of compounds with specific pharmacological properties.
Used in Chemical Biology Studies:
1-BENZYLPYRROLIDIN-3-YL-METHANOL is employed in chemical biology studies aimed at understanding the interactions between small molecules and biological targets. Its structural features facilitate the discovery of new drugs for various therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5731-17-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5731-17:
(6*5)+(5*7)+(4*3)+(3*1)+(2*1)+(1*7)=89
89 % 10 = 9
So 5731-17-9 is a valid CAS Registry Number.

5731-17-9 Well-known Company Product Price

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  • Aldrich

  • (ADE000012)  1-Benzylpyrrolidin-3-yl-methanol  AldrichCPR

  • 5731-17-9

  • ADE000012-1G

  • 1,611.09CNY

  • Detail

5731-17-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzylpyrrolidine-3-methanol

1.2 Other means of identification

Product number -
Other names 1-BENZYLPYRROLIDIN-3-YL-METHANOL

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:5731-17-9 SDS

5731-17-9Relevant articles and documents

Discovery of phenylpyrrolidine derivatives as a novel class of retinol binding protein 4 (RBP4) reducers

Nakamura, Shinji,Kamaura, Masahiro,Akao, Yuichiro,Nakamura, Natsuko,Mizukami, Atsushi,Goto, Akihiko,Furuyama, Naoki,Cho, Nobuo,Kasai, Shizuo

supporting information, (2021/12/30)

Retinol-binding protein 4 (RBP4) is a potential drug target for metabolic and ophthalmologic diseases. A high-throughput screening of our compound library has identified a small-molecule RBP4 reducer 7a, as a hit compound. Aiming to provide a suitable too

Design, synthesis, and characterization of novel, nonquaternary reactivators of GF-inhibited human acetylcholinesterase

McHardy, Stanton F.,Bohmann, Jonathan A.,Corbett, Michael R.,Campos, Bismarck,Tidwell, Michael W.,Thompson, Paul Marty,Bemben, Chris J.,Menchaca, Tony A.,Reeves, Tony E.,Cantrell Jr., William R.,Bauta, William E.,Lopez, Ambrosio,Maxwell, Donald M.,Brecht, Karen M.,Sweeney, Richard E.,McDonough, John

, p. 1711 - 1714 (2014/04/17)

The goal of this research was to identify structurally novel, non-quaternarypyridinium reactivators of GF (cyclosarin)-inhibited hAChE that possess the capacity to mediate in vitro reactivation of GF-inhibited human acetylcholinesterase (hAChE). New compounds were designed, synthesized and assessed in GF-inhibited hAChE assays. Structure activity relationships for AChE binding and reactivation of GF-inhibited hAChE were developed. Lead compounds from two different chemical series, represented by compounds 17 and 38, displayed proficient in vitro reactivation of GF-inhibited hAChE, while also possessing low inhibition of native enzyme.

Disubstituted pyrimidines as Lck inhibitors

Hunt, Julianne A.,Beresis, Richard T.,Goulet, Joung L.,Holmes, Mark A.,Hong, Xinfang J.,Kovacs, Ernest,Mills, Sander G.,Ruzek, Rowena D.,Wong, Frederick,Hermes, Jeffrey D.,Park, Young-Whan,Salowe, Scott P.,Sonatore, Lisa M.,Wu, Lin,Woods, Andrea,Zaller, Dennis M.,Sinclair, Peter J.

supporting information; experimental part, p. 5440 - 5443 (2010/04/26)

We have developed a family of 4-benzimidazolyl-N-piperazinethyl-pyrimidin-2-amines that are subnanomolar inhibitors of Lck. A subset of these Lck inhibitors, with heterocyclic substituents at the benzimidazole C5, are also low-nanomolar inhibitors of cell

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