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1-Piperidineethanol, benzoate (ester) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19069-56-8

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19069-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19069-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,6 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19069-56:
(7*1)+(6*9)+(5*0)+(4*6)+(3*9)+(2*5)+(1*6)=128
128 % 10 = 8
So 19069-56-8 is a valid CAS Registry Number.

19069-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-phenylcarbonyloxyethyl)piperidine

1.2 Other means of identification

Product number -
Other names 1-benzoyloxy-2-piperidin-1-yl-ethane

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:19069-56-8 SDS

19069-56-8Downstream Products

19069-56-8Relevant academic research and scientific papers

A study of 2-piperidino-1-ethanol and its derivatives as antimicrobial additives to oils

Gamzaeva,Mamedova, P. Sh.,Allakhverdieva,Velieva, G. Kh.,Akhundova,Allakhverdiev

, p. 1577 - 1581 (2009)

Some derivatives of 1-hydroxy-2-pyperidinoethane were studied as antimicrobial additives to lubricant oils.

THE REACTIONS OF 2,2,2-TRICHLORO-1-PHENYLETHANONE WITH O, C AND S NUCLEOPHILES

Hess, Sonia Corina,Nome, Faruk,Zucco, Cesar,Rezende, Marcos Caroli

, p. 3037 - 3046 (2007/10/02)

The reactions of 2,2,2-trichloro-1-phenylethanone with various oxygen, carbon and sulfur nucleophiles were investigated with a view of widening the use of trichloroethanones as acylating agents.

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