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N-{3-[3-(4-phenylpiperazin-1-yl)propoxy]phenyl}acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78702-84-8

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78702-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78702-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,0 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78702-84:
(7*7)+(6*8)+(5*7)+(4*0)+(3*2)+(2*8)+(1*4)=158
158 % 10 = 8
So 78702-84-8 is a valid CAS Registry Number.

78702-84-8SDS

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 N-[3-[3-(4-phenylpiperazin-1-yl)propoxy]phenyl]acetamide

1.2 Other means of identification

Product number -
Other names ACETAMIDE,N-(3-(3-(4-PHENYL-1-PIPERAZINYL)PROPOXY)PHENYL)

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:78702-84-8 SDS

78702-84-8Relevant academic research and scientific papers

Dopamine Autoreceptor Agonists as Potential Antipsychotics. 1. (Aminoalkoxy)anilines

Jaen, Juan C.,Wise, Lawrence D.,Heffener, Thomas G.,Pugsley, Thomas A.,Meltzer, Leonard T.

, p. 1621 - 1625 (2007/10/02)

The synthesis and pharmacological properties of a novel type of anilines with dopaminergic properties are described.One of these compounds, 3-benzeneamine (4c), has been identified as a selective

Synthesis and Structure Activity Relationship in 1-(Substituted aminophenoxy)-3-1-(N4-arylpiperazinyl)>propanes

Agarwal, Shiv K.,Saxena, Anil K.,Jain, Padam C.,Anand, Nitya

, p. 914 - 918 (2007/10/02)

1-(Aminophenoxy)-3-1-(N4-arylpiperazinyl)>propanes (1-8) have been prepared by the catalytic hydrogenation of 1-(nitrophenoxy)-3-1-(N4-arylpiperazinyl)>propanes.The reaction of aminophenoxypiperazinylpropanes (1-8) with acetic anhydride gives the corresponding 1-(acetamidophenoxy)-3-1-(N4-arylpiperazinyl)>propanes (9-15) and with methanesulphonyl chloride the corresponding 1-(methanesulfonamidophenoxy)-3-1-(N4-arylpiperazinyl)>propanes (16-19) are obtained.The amino compounds (3 and 4) on treatment with lactim thioethers and isocyanates/isothiocanates afford the corresponding 1-- (20-30) and 1-(ureido/thioureidophenoxy)-3-1-(N44-arylpiperazinyl)>propanes (31-37).Some of these compunds show potent CNS depressant, hypotensive, α-adrenoceptor blocking, antiinflammatory and diuretic activities.Among these compounds 1-(4-aminophenoxy)-3-1-(N4-(2-methoxyphenyl)piperazinyl)>propane (4) is found to be potent neuroleptic.

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