Welcome to LookChem.com Sign In|Join Free

CAS

  • or

561303-39-7

Post Buying Request

561303-39-7 Suppliers

Recommended suppliersmore

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

561303-39-7 Usage

Molecular structure

A piperazinecarboxylic acid derivative with a phenylmethyl group, a propynyl group, and a methyl ester.

Potential pharmaceutical properties

Neuroprotective and anti-inflammatory agent

Possible applications

Treatment of neurological disorders and inflammatory diseases

Specific mechanisms of action

Under investigation

Current status

Under investigation for potential therapeutic uses

Unique chemical structure

Makes it a subject of interest in the field of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 561303-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,1,3,0 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 561303-39:
(8*5)+(7*6)+(6*1)+(5*3)+(4*0)+(3*3)+(2*3)+(1*9)=127
127 % 10 = 7
So 561303-39-7 is a valid CAS Registry Number.

561303-39-7SDS

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 methyl 4-benzyl-3,6-dioxo-2-prop-2-ynylpiperazine-1-carboxylate

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:561303-39-7 SDS

561303-39-7Downstream Products

561303-39-7Relevant articles and documents

Synthesis of 2,6-bridged piperazine-3-ones by N-acyliminium ion chemistry

Veerman, Johan J. N.,Bon, Robin S.,Hue, Bui T. B.,Girones, Daniel,Rutjes, Floris P. J. T.,Van Maarseveen, Jan H.,Hiemstra, Henk

, p. 4486 - 4494 (2007/10/03)

Several 2-substituted and 2,5-disubstituted piperazine-3,6-diones were synthesized starting from readily available α-amino acids. After activation of a lactam carbonyl via introduction of a methoxycarbonyl group onto nitrogen, this carbonyl was selectively reduced. Treatment of the resulting urethane with protic acid generated the corresponding N-acyliminium ion, which was trapped by a nucleophilic C2-side chain to provide 2,6-bridged piperazine-3-ones. Several aromatic, heteroaromatic, and nonaromatic side chains were used as π-nucleophiles. In addition, the effect of the presence of a C5-methyl group on the stereochemical outcome of the cyclization was examined.

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 561303-39-7