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3-Ethoxycarbonylmethyl-piperazine-1-carboxylic acid tert-butyl ester is a chemical compound that belongs to the class of piperazine carboxylic acid esters. It is characterized by a molecular formula of C13H24N2O4 and a molecular weight of 276.34 g/mol. This white to off-white solid has a melting point of 48-51°C and is primarily recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure, featuring a piperazine ring, is a common motif in many bioactive molecules, which may also lend it potential applications in medicinal chemistry and drug development.

849547-86-0

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849547-86-0 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Ethoxycarbonylmethyl-piperazine-1-carboxylic acid tert-buty酯 is used as an intermediate in the production of various drugs. Its unique chemical structure allows it to be a key component in the synthesis of a range of pharmaceuticals, contributing to the development of new medications.
Used in Agrochemical Production:
In the agrochemical industry, 3-ETHOXYCARBONYLMETHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER serves as an intermediate, playing a crucial role in the synthesis of various agrochemicals. Its application helps in the development of products designed to protect crops and enhance agricultural productivity.
Used as a Reagent in Organic Synthesis:
Beyond its applications in pharmaceuticals and agrochemicals, 3-Ethoxycarbonylmethyl-piperazine-1-carboxylic acid tert-butyl ester can also be utilized as a reagent in organic synthesis. Its versatility in chemical reactions makes it a valuable tool for researchers and chemists working on the development of new organic compounds.
Used in Medicinal Chemistry and Drug Development:
Due to its piperazine ring structure, which is prevalent in numerous bioactive molecules, 3-Ethoxycarbonylmethyl-piperazine-1-carboxylic acid tert-butyl ester may have potential applications in medicinal chemistry. It could be instrumental in the discovery and development of new drugs, particularly those targeting specific biological pathways or receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 849547-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,5,4 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 849547-86:
(8*8)+(7*4)+(6*9)+(5*5)+(4*4)+(3*7)+(2*8)+(1*6)=230
230 % 10 = 0
So 849547-86-0 is a valid CAS Registry Number.

849547-86-0SDS

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 3-(2-ethoxy-2-oxoethyl)piperazine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 3-ETHOXYCARBONYLMETHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL 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:849547-86-0 SDS

849547-86-0Downstream Products

849547-86-0Relevant academic research and scientific papers

Identification of MK-5710 ((8aS)-8a-methyl-1,3-dioxo-2-[(1S,2R)-2- phenylcyclopropyl]-N-(1-phenyl-1H-pyrazol-5-yl)hexahydroimid azo[1,5-a]pyrazine-7(1H)-carboxamide), a potent smoothened antagonist for use in Hedgehog pathway dependent malignancies, Part 1

Malancona, Savina,Altamura, Sergio,Filocamo, Gessica,Kinzel, Olaf,Hernando, Jose Ignacio Martin,Rowley, Michael,Scarpelli, Rita,Steinkuehler, Christian,Jones, Philip

, p. 4422 - 4428 (2011)

The Hedgehog (Hh-) signaling pathway is a key developmental pathway which controls patterning, growth and cell migration in most tissues, but evidence has accumulated showing that many human tumors aberrantly reactivate this pathway. Smoothened antagonists offer opportunities for the treatment of malignancies dependent on the Hh pathway, and the most advanced clinical candidates are demonstrating encourage initial results. A novel series of [6,5]-bicyclic tetrahydroimidazo[1,5-a]pyrazine-1,3(2H,5H)-dione smoothened antagonists has been identified, and the series has been extensively explored to ascertain the key detriments for activity, demonstrating that the trans-2-phenylcyclopropyl and hydantoin ring systems are critical for potency, while a variety of urea substituents can be tolerated. The combination of these optimal groups gives smoothened antagonists with activity in the low nanomolar range.

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