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(2R,3R)-PIPERAZINE-2,3-DICARBOXYLIC ACID is a white crystalline solid at room temperature, belonging to the class of piperazine derivatives. It is soluble in water and has two asymmetric carbon centers, resulting in four possible stereoisomers, with the (2R,3R) configuration being one of them. Piperazine derivatives have been studied for their potential pharmaceutical properties, including their use as central nervous system stimulants and their potential as anti-inflammatory agents. Additionally, they have been investigated for their potential as building blocks for organic synthesis. Overall, (2R,3R)-PIPERAZINE-2,3-DICARBOXYLIC ACID has potential applications in pharmaceutical and chemical industries.

46027-28-5

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46027-28-5 Usage

Uses

Used in Pharmaceutical Industry:
(2R,3R)-PIPERAZINE-2,3-DICARBOXYLIC ACID is used as a pharmaceutical compound for its potential as a central nervous system stimulant and anti-inflammatory agent.
Used in Chemical Industry:
(2R,3R)-PIPERAZINE-2,3-DICARBOXYLIC ACID is used as a building block for organic synthesis in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 46027-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,0,2 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 46027-28:
(7*4)+(6*6)+(5*0)+(4*2)+(3*7)+(2*2)+(1*8)=105
105 % 10 = 5
So 46027-28-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2O4/c9-5(10)3-4(6(11)12)8-2-1-7-3/h3-4,7-8H,1-2H2,(H,9,10)(H,11,12)/t3-,4-/m1/s1

46027-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2RS,3RS)-piperazine-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names (+/-)-trans-piperazine-2,3-dicarboxylic acid

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:46027-28-5 SDS

46027-28-5Upstream product

46027-28-5Relevant academic research and scientific papers

Synthesis and pharmacology of N1-substituted piperazine-2,3-dicarboxylic acid derivatives acting as NMDA receptor antagonists

Morley, Richard M.,Tse, Heong-Wai,Feng, Bihua,Miller, Jacqueline C.,Monaghan, Daniel T.,Jane, David E.

, p. 2627 - 2637 (2007/10/03)

The binding site for competitive NMDA receptor antagonists is on the NR2 subunit, of which there are four types (NR2A-D). Typical antagonists such as (R)-AP5 have a subunit selectivity of NR2A > NR2B > NR2C > NR2D. The competitive NMDA receptor antagonist

Hydroformylation of olefins using azoxy-dentated ligands

-

, (2008/06/13)

At a temperature in the range 100° C to 225° C the destructive dissociation of cobalt carbonyl compounds to cobalt metal and residue is inhibited by the action of one or more azoxy-dentated chelation ligands.

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