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Piperazine, 1-ethyl-3-phenyl-, also known as 1-ethyl-3-phenylpiperazine or phenylpiperazine, is an organic compound with the chemical formula C12H18N2. It is a derivative of piperazine, a heterocyclic amine with two nitrogen atoms in a six-membered ring. The molecule features an ethyl group attached to the nitrogen at position 1 and a phenyl group attached to the nitrogen at position 3. Piperazine, 1-ethyl-3-phenyl- is a colorless to pale yellow liquid with a mild, amine-like odor. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its potential psychoactive effects, it is also a controlled substance in some countries.

5271-30-7

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5271-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5271-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5271-30:
(6*5)+(5*2)+(4*7)+(3*1)+(2*3)+(1*0)=77
77 % 10 = 7
So 5271-30-7 is a valid CAS Registry Number.

5271-30-7SDS

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-ethyl-3-phenylpiperazine

1.2 Other means of identification

Product number -
Other names F2147-0777

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:5271-30-7 SDS

5271-30-7Relevant academic research and scientific papers

Biocatalytic Access to Piperazines from Diamines and Dicarbonyls

Borlinghaus, Niels,Gergel, Sebastian,Nestl, Bettina M.

, p. 3727 - 3732 (2018)

Given the widespread importance of piperazines as building blocks for the production of pharmaceuticals, an efficient and selective synthesis is highly desirable. Here we show the direct synthesis of piperazines from 1,2-dicarbonyl and 1,2-diamine substrates using the R-selective imine reductase from Myxococcus stipitatus as biocatalyst. Various N- and C-substituted piperazines with high activity and excellent enantioselectivity were obtained under mild reaction conditions reaching up to 8.1 g per liter.

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