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1-Propanone, 1-(4-hydroxyphenyl)-3-(1-piperidinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42528-76-7

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42528-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42528-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,2 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42528-76:
(7*4)+(6*2)+(5*5)+(4*2)+(3*8)+(2*7)+(1*6)=117
117 % 10 = 7
So 42528-76-7 is a valid CAS Registry Number.

42528-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-hydroxyphenyl)-3-piperidin-1-ylpropan-1-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:42528-76-7 SDS

42528-76-7Relevant academic research and scientific papers

Evaluation of Cytotoxic Properties of N,N'-bis[(1-aryl-3-heteroaryl)propylidene]-hydrazine dihydrochlorides

Kucukoglu,Gul,Sakagami

, p. 784 - 787 (2020/11/23)

N,N'-bis[(1-aryl-3-heteroaryl)propylidene]hydrazine dihydrochlorides, P1, P4 – P8, and R1 – R7, were assayed against human oral squamous cell carcinoma (HSC-2, HSC-3, HSC-4), human promyelocytic leukemia cell line (HL-60), and human normal oral cells (HGF

Design, synthesis and evaluation of tacrine based acetylcholinesterase inhibitors

Shen, Yanhong,Yu, Youzhu,Lv, Huichao,Feng, Liping,Zhang, Guoqiang

scheme or table, p. 341 - 345 (2011/10/18)

A series of tacrine based cholinesterase inhibitors was designed, synthesized and assayed for their biological activity. Among them, five compounds inhibited acetylcholinesterase in micromolar range and most of the compounds demonstrated much better selectivity for AChE than reference compound tacrine.

2-Phenoxy-indan-1-one derivatives as acetylcholinesterase inhibitors: A study on the importance of modifications at the side chain on the activity

Shen, Yanhong,Sheng, Rong,Zhang, Jing,He, Qiaojun,Yang, Bo,Hu, Yongzhou

, p. 7646 - 7653 (2008/12/23)

As a part of our project aimed at developing new agents of potential application in AD, a new series of 2-phenoxy-indan-1-one derivatives which possess alkylamine side chain were designed, synthesized, and evaluated for their inhibitory activity against AChE and BuChE. Most of the compounds were found to inhibit AChE in the nanomolar range. The optimum inhibitor 3g exhibited 34-fold increase in AChE inhibition than donepezil and displayed neuroprotective effect against H2O2-induced cell death.

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