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4-Carbamyl-1-piperazinecarboxylic acid benzyl ester is a chemical compound with the molecular formula C14H18N2O4. It is an ester derivative of 4-carbamyl-1-piperazinecarboxylic acid, where the carboxylic acid group is esterified with benzyl alcohol. 4-Carbamyl-1-piperazinecarboxylic acid benzyl ester is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs and medicinal agents. Its structure features a piperazine ring, a carbamate group, and a benzyl ester moiety, which contribute to its reactivity and functional group chemistry. The compound is often used in the synthesis of drugs targeting the central nervous system, such as antidepressants and antipsychotics, due to its ability to form stable intermediates and its potential to modulate neurotransmitter activity.

588-88-5

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588-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 588-88-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 588-88:
(5*5)+(4*8)+(3*8)+(2*8)+(1*8)=105
105 % 10 = 5
So 588-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H17N3O3/c14-12(17)11-3-1-10(2-4-11)9-19-13(18)16-7-5-15-6-8-16/h1-4,15H,5-9H2,(H2,14,17)

588-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-carbamoyl-piperazine-1-carboxylic acid benzyl ester

1.2 Other means of identification

Product number -
Other names 4-(aminocarbonyl)-1-piperazinecarboxylic acid,phenylmethyl ester

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:588-88-5 SDS

588-88-5Downstream Products

588-88-5Relevant academic research and scientific papers

Regioselective Formal [3+2] Cycloadditions of Urea Substrates with Activated and Unactivated Olefins for Intermolecular Olefin Aminooxygenation

Wu, Fan,Alom, Nur-E,Ariyarathna, Jeewani P.,Na?, Johannes,Li, Wei

supporting information, p. 11676 - 11680 (2019/07/31)

A new class of intermolecular olefin aminooxygenation reaction is described. This reaction utilizes the classic halonium intermediate as a regio- and stereochemical template to accomplish the selective oxyamination of both activated and unactivated alkenes. Notably, urea chemical feedstock can be directly introduced as the N and O source and a simple iodide salt can be utilized as the catalyst. This formal [3+2] cycloaddition process provides a highly modular entry to a range of useful heterocyclic products with excellent selectivity and functional-group tolerance.

Beta lactam compounds and their use as inhibitors of tryptase

-

Page column 154, (2010/11/29)

Compounds of the formulas: are disclosed. These compounds inhibit tryptase as well as other enzyme systems or are selective tryptase inhibitors and are useful as antiinflammatory agents particularly in the treatment of chronic asthma.

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