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Benzoic acid, 4-[4-(phenylmethyl)-1-piperazinyl]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94038-25-2

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94038-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94038-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,3 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94038-25:
(7*9)+(6*4)+(5*0)+(4*3)+(3*8)+(2*2)+(1*5)=132
132 % 10 = 2
So 94038-25-2 is a valid CAS Registry Number.

94038-25-2SDS

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 ethyl 4-(4-benzylpiperazin-1-yl)benzoate

1.2 Other means of identification

Product number -
Other names 4-(4-BENZYL-1-PIPERAZINYL)BENZOIC ACID ETHYL 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:94038-25-2 SDS

94038-25-2Relevant academic research and scientific papers

Base-Mediated Oxidative Degradation of Secondary Amides Derived from p-Amino Phenol to Primary Amides in Drug Molecules

Nanda, Kausik K.,Ginnetti, Anthony,Wuelfing, W. Peter

, p. 3394 - 3403 (2020/08/19)

One of the most common functional groups encountered in drug molecules is the amide, and the most common degradation pathway for amides is base-mediated hydrolysis to its constituent amine and carboxylic acid. Herein, we report for the first time, a base-

PIPERIDINE/PIPERAZINE DERIVATIVES

-

Page/Page column 72, (2009/01/24)

The invention further relates to a DGAT inhibitor of formula (I), including any stereochemically isomeric form thereof, wherein A represents CH or N; the dotted line represents an optional bond in case A represents a carbon atom; X represents -NRx -C(=O)-; -Z-C(=O)-; -Z-NRx -C(=O)-; -S(=O)p-; C(=S)-; -NRx -C(=S)-; -Z-C(=S)-; -Z-NRx -C(=S)-; -O-C(=O)-; -C(=O)-C(=O)-; R1 represents a 5-membered monocyclic heterocycle containing at least 2 heteroatoms; a 6-membered aromatic monocyclic heterocycle; or a 5-membered heterocycle containing at least 2 heteroatoms fused with phenyl, cyclohexyl or a 5-or 6-membered heterocycle; wherein each of said heterocycles may optionally be substituted; R2 represents R3; R3 represents C3-6cycloalkyl, phenyl, naphtalenyl, 2,3-dihydro-1,4-benzodioxinyl, 1,3-benzodioxolyl, 2,3-dihydrobenzofuranyl or a 6-membered aromatic heterocycle containing 1 or 2 N atoms,wherein said C3-6cycloalkyl, phenyl, naphtalenyl, 2,3-dihydro-1,4-benzo- dioxinyl, 1,3-benzodioxolyl,2,3-dihydrobenzofuranyl or 6-membered aromatic heterocycle may optionally be substituted; a N-oxide thereof, a pharmaceutically acceptable salt thereof or a solvate thereof. The invention further relates to methods for preparing such compounds, pharmaceutical compositions comprising said compounds as well as the use as a medicine of said compounds.

Anti-virally active pyridazinamines

-

, (2008/06/13)

Anti-virally active pyridazinamines, compositions containing the same and methods of treating viral diseases in warm-blooded animals.

High pressure organic chemistry; XII. A convenient synthesis of aromatic amines from activated aromatic fluorides

Kotsuki,Kobayashi,Matsumoto,Suenaga,Nishizawa

, p. 1147 - 1148 (2007/10/02)

Aromatic fluorides containing electron-withdrawing substituents are cleanly reacted with amines at 10 kbar pressure to give various aromatic amines.

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