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1-(piperazin-1-yl)-2-propylpentan-1-one is a chemical compound with the molecular formula C12H24N2O. It is a derivative of pentanone, featuring a piperazine ring attached to the first carbon atom and a propyl group on the second carbon. 1-(piperazin-1-yl)-2-propylpentan-1-one is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs and medicinal agents. Its structure allows for the formation of diverse chemical entities, making it a valuable intermediate in organic synthesis. The compound's properties, such as solubility and reactivity, can be influenced by the presence of the piperazine ring, which can engage in hydrogen bonding and other interactions. This versatility makes 1-(piperazin-1-yl)-2-propylpentan-1-one an important component in the development of new chemical entities with potential therapeutic applications.

3116-35-6

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3116-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3116-35-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3116-35:
(6*3)+(5*1)+(4*1)+(3*6)+(2*3)+(1*5)=56
56 % 10 = 6
So 3116-35-6 is a valid CAS Registry Number.

3116-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-piperazin-1-yl-2-propylpentan-1-one

1.2 Other means of identification

Product number -
Other names 2-Propyl-valeriansaeure-piperazid

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:3116-35-6 SDS

3116-35-6Downstream Products

3116-35-6Relevant academic research and scientific papers

Efficient Synthesis of Benzothiazinone Analogues with Activity against Intracellular Mycobacterium tuberculosis

Richter, Adrian,Narula, Gagandeep,Rudolph, Ines,Seidel, Rüdiger W.,Wagner, Christoph,Av-Gay, Yossef,Imming, Peter

supporting information, (2021/12/27)

8-Nitrobenzothiazinones (BTZs) are a promising class of antimycobacterial agents currently under investigation in clinical trials. Starting from thiourea derivatives, a new synthetic pathway to BTZs was established. It allows the formation of the thiazinone ring system in one synthetic step and is applicable for preparation of a wide variety of BTZ analogues. The synthetic procedure furthermore facilitates the replacement of the sulphur atom in the thiazinone ring system by oxygen or nitrogen to afford the analogous benzoxazinone and quinazolinone systems. 36 BTZ analogues were prepared and tested in luminescence-based assays for in vitro activity against Mycobacterium tuberculosis (Mtb) using the microdilution broth method and a high-throughput macrophage infection assay.

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