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1-[2-[(2-aminoethyl)amino]ethyl]pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6258-05-5

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6258-05-5 Usage

Chemical structure

A derivative of pyrrolidine with an amine and an ethyl group attached

Applications

a. Synthesis of various pharmaceuticals and organic compounds
b. Potential candidate for drug development due to its pharmacological properties
c. Research and development of new chemical entities

Safety precautions

Requires careful handling and proper safety measures in laboratory settings due to its complex molecular structure

Check Digit Verification of cas no

The CAS Registry Mumber 6258-05-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,5 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6258-05:
(6*6)+(5*2)+(4*5)+(3*8)+(2*0)+(1*5)=95
95 % 10 = 5
So 6258-05-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H19N3/c9-3-4-10-5-8-11-6-1-2-7-11/h10H,1-9H2

6258-05-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(2-pyrrolidin-1-ylethyl)ethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names EINECS 228-389-4

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:6258-05-5 SDS

6258-05-5Downstream Products

6258-05-5Relevant academic research and scientific papers

Dehydrogenative Coupling of Ethanol and Ester Hydrogenation Catalyzed by Pincer-Type YNP Complexes

Gusev, Dmitry G.

, p. 6967 - 6981 (2016/10/14)

The "Y" donor group (Y = -OMe, -SEt, -PPh2, -NH2, -NMe2, -Py, pyrrolidinyl, quinolyl) of the pincer-type ruthenium complexes RuHCl(CO)[κ3-YNP] has a dramatic influence on the catalytic activity in the dehydrogenative homocoupling and cross-coupling of ethanol and ester hydrogenation reactions. The observations are connected with the mechanisms of the catalytic reactions, and this paper provides evidence for ester C-O bond formation/cleavage assisted by the bifunctional catalysts in an outer-sphere fashion, reminiscent of the Tishchenko chemistry.

DIUREA DERIVATIVES

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Page/Page column 14-15, (2008/06/13)

The present invention relates to novel diurea derivatives that block intracellular signal transduction and thereby inhibit the production of pro-inflammatory cytokines, especially interleukin-2 (IL-2) and/or induce apoptosis in activated T-cells. It further discloses such a compound for use as a medicament, the use of said compound for the manufacturing of a medicament for the treatment of immune disorders which benefit from inhibition of production of IL-2 and other pro-inflammatory cytokines and/or induction of apoptosis in activated T-cells, a pharmaceutical composition comprising said compound and a method of treatment comprising administration of a pharmaceutically effective amount of said compound. A compound of the general formula I.

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