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(3-PIPERAZIN-1-YL-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER is a chemical compound that serves as a versatile reagent in pharmaceutical research and synthesis. It is an ester derivative of carbamic acid, characterized by the presence of a piperazine ring, which endows it with distinctive pharmacological properties. The tert-butyl ester group attached to the carbamic acid contributes to the molecule's stability and ease of handling in laboratory conditions.

874831-60-4

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874831-60-4 Usage

Uses

Used in Pharmaceutical Research and Synthesis:
(3-PIPERAZIN-1-YL-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER is used as an intermediate in the synthesis of various pharmaceutical drugs due to its unique chemical structure and reactivity.
Used in Organic Reactions:
In the field of organic chemistry, (3-PIPERAZIN-1-YL-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER is utilized as a catalyst to facilitate specific reactions, enhancing the efficiency and selectivity of the processes.
Used in Therapeutic Agent Development:
(3-PIPERAZIN-1-YL-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER has been studied for its potential as a therapeutic agent, indicating its broad applications in the treatment of various diseases, although specific applications would require further research and clinical validation.
Used in Laboratory Settings:
The stability and protective nature of the tert-butyl ester group allow (3-PIPERAZIN-1-YL-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER to be easily manipulated in laboratory settings, making it a valuable tool for researchers in the development of new chemical entities and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 874831-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,8,3 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 874831-60:
(8*8)+(7*7)+(6*4)+(5*8)+(4*3)+(3*1)+(2*6)+(1*0)=204
204 % 10 = 4
So 874831-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H25N3O2/c1-12(2,3)17-11(16)14-5-4-8-15-9-6-13-7-10-15/h13H,4-10H2,1-3H3,(H,14,16)

874831-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(3-piperazin-1-ylpropyl)carbamate

1.2 Other means of identification

Product number -
Other names 1-(3-n-boc-aminopropyl)-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:874831-60-4 SDS

874831-60-4Downstream Products

874831-60-4Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR THE TREATMENT OF HUMAN IMMUNODEFICIENCY VIRUS

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Page/Page column 337, (2020/12/30)

Compositions and methods for the treatment of viral infections include conjugates containing inhibitors of viral gp120 receptor (e.g., temsavir, BMS-818251, DMJ-ll-121, BNM-IV-147, or analogs thereof) linked to an Fc monomer, an Fc domain, and Fc-binding peptide, an albumin protein, or albumin- binding peptide. In particular, conjugates can be used in the treatment of viral infections (e.g., HIV infections).

SUBSTITUTED PYRIDINES AS INHIBITORS OF DNMT1

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, (2018/01/20)

The invention is directed to substituted pyridine derivatives. Specifically, the invention is directed to compounds according to Formula (Iar): (Iar) wherein Yar, X1ar, X2ar, R1ar, R2ar, R3ar, R4ar and R5ar are as defined herein; or a pharmaceutically acceptable salt or prodrug thereof. The compounds of the invention are selective inhibitors of DNMT1 and can be useful in the treatment of cancer, pre-cancerous syndromes, beta hemoglobinopathy disorders, sickle cell disease, sickle cell anemia, and beta thalassemia, and diseases associated with DNMT1 inhibition. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting DNMT1 activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

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