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14340-32-0

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14340-32-0 Usage

Type of compound

Phenylpiperazine derivative

Usage

Precursor in the synthesis of pharmaceuticals and research chemicals

Applications

Production of antipsychotic and antihistamine drugs, development of novel therapeutic agents

Potential therapeutic benefits

Serotonin antagonist, treatment of anxiety disorders and other mental health conditions

Interest

Researchers and pharmaceutical companies for its potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 14340-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,4 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14340-32:
(7*1)+(6*4)+(5*3)+(4*4)+(3*0)+(2*3)+(1*2)=70
70 % 10 = 0
So 14340-32-0 is a valid CAS Registry Number.

14340-32-0SDS

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 4-phenylpiperazin-1-amine

1.2 Other means of identification

Product number -
Other names 1-amino-4-phenylpiperazine

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:14340-32-0 SDS

14340-32-0Relevant articles and documents

Selective reduction of N-nitroso aza-aliphatic cyclic compounds to the corresponding N-amino products using zinc dust in CO2–H2O medium

Yang, Weiqing,Lu, Xiang,Zhou, Tingting,Cao, Yongjing,Zhang, Yuanyuan,Ma, Menglin

, p. 780 - 783 (2018/10/20)

[Figure not available: see fulltext.] A new method for reduction of N-nitroso aza-aliphatic cyclic compounds employing zinc in pressurized CO2–H2O medium has been developed. H2O and NH4Cl were used as hydrogen donors, and reduction was performed under environmentally benign conditions. The presented approach allowed to obtain the respective N-amino products selectively and in excellent yields (up to 97%).

NEW DRUGS WITH ANTICHOLESTATIC ACTIVITY

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Page/Page column 19, (2009/03/07)

New compounds belonging to the structural formula (I) are described. formula (I) in which R1, R2, A, Y and X are specified in the description, useful in the treatment of cholestasis and substantially devoid of antibacterial activity. The synthesis process of said compounds, the pharmaceutical compositions containing them and their use in therapy are also described.

Potential antihypertensive agents. II. Unsymmetrically 1,4-disubstituted piperazines.

Prasad,Hawkins,Tietje

, p. 1144 - 1150 (2007/10/04)

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