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1-(4-Isopropylbenzyl)piperazine, also known as 4-(1-piperazinyl)-isopropylbenzene, is a piperazine-based chemical compound featuring a piperazine ring connected to a benzene ring with an isopropyl group substitution. This versatile compound has been utilized in scientific research as a precursor for the synthesis of various pharmacological agents and is under investigation for potential applications in treating different medical conditions. Additionally, it serves as an intermediate in the production of pharmaceutical drugs and may have a range of other industrial uses. Careful handling and adherence to safety protocols are essential when working with this chemical.

23145-95-1

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23145-95-1 Usage

Uses

Used in Pharmaceutical Research and Development:
1-(4-Isopropylbenzyl)piperazine is used as a precursor in the synthesis of various pharmacological compounds for the development of new medications. Its unique structure allows for the creation of diverse drug candidates with potential therapeutic applications.
Used in Medical Treatments:
1-(4-Isopropylbenzyl)piperazine is being investigated for its potential use in the treatment of various medical conditions. Its specific role in these treatments is still under research, but its chemical properties make it a promising candidate for further study and development.
Used in Industrial Applications:
Beyond its pharmaceutical uses, 1-(4-Isopropylbenzyl)piperazine may also have applications in other industries. Its versatility and chemical properties could make it suitable for a range of purposes, although specific uses would depend on the industry's requirements and the compound's compatibility with other materials and processes.
Used in Drug Synthesis as an Intermediate:
1-(4-Isopropylbenzyl)piperazine is utilized as an intermediate in the synthesis of pharmaceutical drugs. Its role in this process is crucial, as it contributes to the formation of the final drug product, ensuring the desired therapeutic effects and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 23145-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,4 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23145-95:
(7*2)+(6*3)+(5*1)+(4*4)+(3*5)+(2*9)+(1*5)=91
91 % 10 = 1
So 23145-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H22N2/c1-12(2)14-5-3-13(4-6-14)11-16-9-7-15-8-10-16/h3-6,12,15H,7-11H2,1-2H3/p+2

23145-95-1SDS

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 1-[(4-propan-2-ylphenyl)methyl]piperazine

1.2 Other means of identification

Product number -
Other names HMS1783L02

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:23145-95-1 SDS

23145-95-1Relevant academic research and scientific papers

PROCASPASE-ACTIVATING COMPOUNDS AND COMPOSITIONS

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Paragraph 0088; 0165-0166, (2013/04/24)

The invention provides compounds and compositions useful for the modulation of certain enzymes. The compounds and compositions can induce of cell death, particularly cancer cell death. The invention also provides methods for the synthesis and use of the compounds and compositions, including the use of compounds and compositions in therapy for the treatment of cancer and selective induction of apoptosis in cells.

Piperazino-Functionalized Silica Gel as a Deblocking-Scavenging Agent for the 9-Fluorenylmethyloxycarbonyl Amino-Protecting Group

Carpino, Louis A.,Mansour, E. M. E.,Knapczyk, Jerome

, p. 666 - 669 (2007/10/02)

Bonding cyclic secondary amino residues to the surface of silica gel has given insoluble reagents capable of deblocking the 9-fluorenylmethyloxycarbonyl amino-protecting group and at the same time scavenging the dibenzofulvene (DBF) liberated in the deblocking process.A piperazino silica reagent 6 bearing approximately 1.1 mequiv of NH/g was easiest to prepare by reaction of trimethoxysilane 5 with chromatographic-grade silica.After use, spent reagent could be regenerated by treatment with excess piperidine.Piperidino silicas 14 and 15 were made similarly.For the amino-functionalized silica reagents and a variety of simple cyclic secondary amines (piperazine, piperidine, etc.) the existence of an equilibrium (eq 3) between DBF (2) and adduct 7 has been established with the position of equilibrium being dependent on the nature of the amine, solvent, etc.Both deblocking and attainment of equilibrium were faster in Me2SO than in chloroform or dichloromethane.With piperazines in Me2SO the equilibrium was shifted toward complete scavenging by precipitation of the adduct from the reaction medium.

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