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4-(3-FORMYL-4-HYDROXYPHENYL)PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is a piperazine derivative with a molecular formula C17H21N3O4, featuring a formyl group, a hydroxyphenyl group, and a carboxylic acid group. The tert-butyl ester group serves as a protecting group in organic synthesis, preventing unwanted side reactions. 4-(3-FORMYL-4-HYDROXYPHENYL)PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER may hold potential pharmaceutical applications due to the known biological activity of piperazine derivatives, which are utilized in the development of various therapeutic agents.

343306-50-3

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343306-50-3 Usage

Uses

Used in Pharmaceutical Industry:
4-(3-FORMYL-4-HYDROXYPHENYL)PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is used as a potential pharmaceutical agent for its biological activity. Piperazine derivatives, to which 4-(3-FORMYL-4-HYDROXYPHENYL)PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER belongs, are known for their therapeutic potential, and further research may uncover specific applications in medicine.
Used in Organic Synthesis:
In the field of organic synthesis, 4-(3-FORMYL-4-HYDROXYPHENYL)PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is utilized with its tert-butyl ester group acting as a protecting group. This feature allows chemists to carry out reactions without affecting the carboxylic acid functionality, thus facilitating the synthesis of more complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 343306-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,3,0 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 343306-50:
(8*3)+(7*4)+(6*3)+(5*3)+(4*0)+(3*6)+(2*5)+(1*0)=113
113 % 10 = 3
So 343306-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H22N2O4/c1-16(2,3)22-15(21)18-8-6-17(7-9-18)13-4-5-14(20)12(10-13)11-19/h4-5,10-11,20H,6-9H2,1-3H3

343306-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(3-formyl-4-hydroxyphenyl)piperazine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 5-(4-tert-butoxycarbonylpiperazin-1-yl)-2-hydroxybenzaldehyde

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:343306-50-3 SDS

343306-50-3Downstream Products

343306-50-3Relevant academic research and scientific papers

Dual 5-HT1A agonists and 5-HT re-uptake inhibitors by combination of indole-butyl-amine and chromenonyl-piperazine structural elements in a single molecular entity

Heinrich, Timo,B?ttcher, Henning,Schiemann, Kai,H?lzemann, Günter,Schwarz, Michael,Bartoszyk, Gerd D.,Van Amsterdam, Christoph,Greiner, Hartmut E.,Seyfried, Christoph A.

, p. 4843 - 4852 (2004)

A series of compounds such as dual serotonin re-uptake inhibitor and 5-HT1A receptor agonist was found to increase central serotonin levels in rat brain to a greater extent than established antidepressants. The dual serotonin (5-HT) re-uptake i

Method for preparing vilazodone intermediate through copper-catalyzed coupling reaction

-

Paragraph 0037; 0047; 0050-0053; 0056; 0059-0062; 0066; ..., (2021/08/07)

The invention discloses a method for preparing a vilazodone intermediate through a copper-catalyzed coupling reaction. The method comprises the following steps: step 1, generating 2-hydroxy-5-bromobenzene dimethyl acetal (IV) from 2-hydroxy-5-bromobenzald

Benzofurane, benzothiophene, benzothiazol derivatives as FXR modulators

-

Page/Page column 30, (2009/10/31)

The present invention relates to compounds of formula (I) wherein the substituents are as defined in the claims, including pharmaceutical compositions thereof and for their use in the treatment and/or prevention and/or amelioration of one or more symptoms

Method for producing 5-(1-piperazinyl) -benzofuran-2-carboxamide by transition metal-catalyzed amination

-

, (2008/06/13)

1. Process for the preparation of 5-(1-piperazinyl)benzofuran-2-carboxamide in which, as intermediate step, 5-bromosalicylaldehyde or one of its derivatives is reacted in a transition metal-catalysed amination with R2-piperazine, in which R2 is as defined in claim 1.

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