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2-Piperidinone, 1-[[1-methyl-5-[[4-[2-(1-methylpropoxy)phenyl]-1-piperazinyl]methyl]-1H- pyrrol-2-yl]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123547-37-5

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123547-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123547-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,5,4 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123547-37:
(8*1)+(7*2)+(6*3)+(5*5)+(4*4)+(3*7)+(2*3)+(1*7)=115
115 % 10 = 5
So 123547-37-5 is a valid CAS Registry Number.

123547-37-5SDS

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 1-{5-[4-(2-sec-Butoxy-phenyl)-piperazin-1-ylmethyl]-1-methyl-1H-pyrrol-2-ylmethyl}-piperidin-2-one

1.2 Other means of identification

Product number -
Other names -

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:123547-37-5 SDS

123547-37-5Downstream Products

123547-37-5Relevant academic research and scientific papers

Pyrrole Mannich bases as potential antipsychotic agents

Scott,Martin,DiStefano,Fedde,Kukla,Barrett,Baldy,Elgin Jr.,Kesslick,Mathiasen,Shank,Vaught

, p. 552 - 558 (2007/10/02)

Recently, we reported on a series of arylpiperazines 4 which exhibit high affinity for the serotonin 5-HT-1A and 5-HT-1B binding sites. Although these compounds interact weakly with dopamine D-1 and D-2 receptors, they are reasonably potent in inhibiting conditioned avoidance responding (CAR) in the rat, an indication of potential antipsychotic activity. Conversion of these arylpiperazines to pyrrole Mannich bases has provided a series of compounds (10-44) which exhibit potent inhibition of CAR when given po and have strong affinity for both the D-2 and 5-HT-1A binding sites. Some of these agents also fail to produce catalepsy. The D-2 binding data and the block of CAR suggest that they are potential antipsychotic agents and the lack of cataleptogenic potential suggests some might possess less liability for producing extrapyramidal side effects and tardive dyskinesias in man.

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