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1-Pyrrolidin-3-yl-piperidine is a chemical compound that features a piperidine ring connected to a pyrrolidine ring. It serves as a precursor in the synthesis of pharmaceuticals and is instrumental in the development of various drugs. However, it is also recognized as an intermediate in the production of certain illicit substances, which has led to its classification as a controlled substance in some jurisdictions, including the United States where it is listed as a Schedule II controlled substance due to its potential for abuse and addiction. Careful handling and adherence to regulations and safety guidelines are essential when working with 1-PYRROLIDIN-3-YL-PIPERIDINE.

184970-32-9

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184970-32-9 Usage

Uses

Used in Pharmaceutical Industry:
1-Pyrrolidin-3-yl-piperidine is used as a chemical precursor for the synthesis of various pharmaceuticals, playing a crucial role in the development of new drugs. Its unique structure allows it to be a building block in the creation of medicinal compounds that can address a range of health conditions.
Used in Controlled Substances Regulation:
1-Pyrrolidin-3-yl-piperidine is used as a controlled substance in jurisdictions like the United States to prevent its misuse in the production of illicit drugs. As a Schedule II controlled substance, it is subject to strict regulations to mitigate the risk of abuse and addiction.

Check Digit Verification of cas no

The CAS Registry Mumber 184970-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,9,7 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 184970-32:
(8*1)+(7*8)+(6*4)+(5*9)+(4*7)+(3*0)+(2*3)+(1*2)=169
169 % 10 = 9
So 184970-32-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H18N2/c1-2-6-11(7-3-1)9-4-5-10-8-9/h9-10H,1-8H2

184970-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pyrrolidin-3-ylpiperidine

1.2 Other means of identification

Product number -
Other names -

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:184970-32-9 SDS

184970-32-9Relevant academic research and scientific papers

COMPOUNDS FOR INHIBITING CELL PROLIFERATION IN EGFR-DRIVEN CANCERS

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Page/Page column 64, (2013/12/03)

The invention features compounds, pharmaceutical compositions and methods for treating patients who have an EGFR-driven cancer of Formula (I), wherein the variables are as defined herein.

Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds

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, (2008/06/13)

The present invention relates to alkyne compounds of general formula I wherein the groups and residues A, B, W, X, Y, Z, R1 and R2 have the meanings given in claim 1. The invention further relates to pharmaceutical compositions containing at least one alkyne according to the invention. In view of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.

3-[4-Substituted heterocyclyl)-pyrrol-2-ylmethylidene]-2- indolinone derivatives as kinase inhibitors

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, (2008/06/13)

The present invention relates to certain 3-[4-(substituted heterocyclyl)-pyrrol-2-ylmethylidene]-2-indolinone derivatives that inhibit kinases, in particular VEGFR and/or PDGFR kinases. Pharmaceutical compositions comprising these compounds, methods of treating diseases mediated by kinases utilizing pharmaceutical compositions comprising these compounds, and methods of preparing them are also disclosed.

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