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(9H-Fluoren-9-yl)methyl 4-(4-aminophenyl)piperazine-1-carboxylate is a complex organic molecule characterized by the presence of a fluorenyl-methyl group attached to a 4-(4-aminophenyl)piperazine-1-carboxylate. The fluorenyl-methyl group is a substituted fluorene, a polycyclic aromatic hydrocarbon, while the piperazine-1-carboxylate is a substituted piperazine, a heterocyclic organic compound. This unique structure suggests potential applications in various industries, particularly in pharmaceuticals and materials science, due to the presence of the piperazine moiety, which is a common structural element in many bioactive compounds and drugs.

412331-98-7

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412331-98-7 Usage

Uses

Used in Pharmaceutical Industry:
(9H-Fluoren-9-yl)methyl 4-(4-aminophenyl)piperazine-1-carboxylate is used as a building block for the synthesis of various bioactive compounds and drugs. Its unique structure, including the fluorenyl-methyl and piperazine-1-carboxylate groups, allows for the development of new pharmaceutical agents with potential therapeutic applications.
Used in Materials Science:
(9H-Fluoren-9-yl)methyl 4-(4-aminophenyl)piperazine-1-carboxylate is used as a component in the development of advanced materials with specific properties. The presence of the fluorenyl-methyl group and the heterocyclic piperazine-1-carboxylate group may contribute to the creation of materials with unique characteristics, such as improved stability, conductivity, or other desirable properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 412331-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,3,3 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 412331-98:
(8*4)+(7*1)+(6*2)+(5*3)+(4*3)+(3*1)+(2*9)+(1*8)=107
107 % 10 = 7
So 412331-98-7 is a valid CAS Registry Number.

412331-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-aminophenyl)-piperazine-1-carboxylic acid 9H-fluoren-9-ylmethyl ester

1.2 Other means of identification

Product number -
Other names 4-(4-Amino-phenyl)-piperazine-1-carboxylic acid 9H-fluoren-9-ylmethyl 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:412331-98-7 SDS

412331-98-7Downstream Products

412331-98-7Relevant academic research and scientific papers

Synthesis and evaluation of a novel series of farnesyl protein transferase inhibitors as non-peptidic CAAX tetrapeptide analogues

Perez, Michel,Maraval, Catherine,Dumond, Stephan,Lamothe, Marie,Schambel, Philippe,Etievant, Chantal,Hill, Bridget

, p. 1455 - 1458 (2007/10/03)

A novel series of compounds, derived from 4-amino-phenyl piperazine, has been designed to selectively inhibit farnesyl protein transferase (FPTase) as CAAX tetrapeptide analogues. Certain of these compounds were shown to possess low nanomolar inhibitory a

Automated commercial synthesis system for preparation of O-(2-[18F]fluoroethyl)-L-tyrosine by direct nucleophilic displacement on a resin column

Tang, Ganghua,Tang, Xiaolan,Wang, Mingfang,Luo, Lei,Gan, Manquan,Huang, Zuhan

, p. 645 - 660 (2007/10/03)

A slightly modified automated commercial synthesis system for preparation of O-(2-[18F]fluoroethyl)-L-tyrosine (FET), an amino acid tracer for tumor imaging with positron emission tomography, is described. Direct nucleophilic fluorination of [18F]fluoride

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