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507263-18-5

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507263-18-5 Usage

Structure

An ester derivative of 4-(3-methoxyphenyl)-1-piperazinecarboxylic acid

Usage

Commonly used in pharmaceutical research and development

Therapeutic potential

Studied for potential effects on various diseases and conditions, including neurological disorders and psychiatric illnesses

Possible applications

Antipsychotic or antidepressant agent, treatment of other mental health conditions

Synthesis use

May be used as a precursor or intermediate in the synthesis of other pharmaceutical compounds

Check Digit Verification of cas no

The CAS Registry Mumber 507263-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,7,2,6 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 507263-18:
(8*5)+(7*0)+(6*7)+(5*2)+(4*6)+(3*3)+(2*1)+(1*8)=135
135 % 10 = 5
So 507263-18-5 is a valid CAS Registry Number.

507263-18-5SDS

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 1-(tert-butoxycarbonyl)-4-(3-methoxyphenyl)piperazine

1.2 Other means of identification

Product number -
Other names 1-tert-butoxycarbonyl-4-(3-methoxyphenyl)piperazine

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:507263-18-5 SDS

507263-18-5Relevant articles and documents

Synthesis of fluorescein derivatives containing metal-coordinating heterocycles

Clark, Matthew A.,Hilderbrand, Scott A.,Lippard, Stephen J.

, p. 7129 - 7131 (2004)

Fluorescein derivatives that contain Lewis basic heterocycles have been synthesized by concise reaction sequences. The preparation of these compounds proceeds by functionalization of an electron-rich aromatic precursor and subsequent condensation to form the fluorophore. These compounds are envisioned as components of metal-based sensors.

A class of GPR40 agonist compounds with amide structure, and uses thereof

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Paragraph 0145; 0146; 0147; 0148; 0150, (2019/05/02)

The present invention relates to a class of amide compounds with a novel structure, and a pharmaceutical composition thereof, wherein the structure of the amide compound is represented by a general formula (I). According to the present invention, the amide compound (I) can regulate GPR40 activity, and can be used for GPR40 activity related diseases such as diabetes and metabolic syndrome. The formula I is defined in the specification.

SUBSTITUTED 2-AMINOPYRIDINE PROTEIN KINASE INHIBITOR

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Paragraph 0098, (2015/12/19)

Disclosed are a 2-aminopyridine derivative having protein kinase inhibition activity, a preparation method and a pharmaceutical composition thereof Also disclosed are uses of the compounds and the pharmaceutical compositions thereof in the preparation of drugs for treating and/or preventing protein kinase-related diseases.

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