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4593-17-3

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4593-17-3 Usage

Type

Chemical compound

Derivative of

Piperidine

Industry use

Pharmaceutical industry

Building block for

Synthesis of various drugs

Properties

Analgesic and anesthetic

Potential use

Local anesthetic

Investigated for

Treatment of drug addiction

Application

Studying the central nervous system

Role

Significant in medicinal chemistry

Applications

Various fields

Check Digit Verification of cas no

The CAS Registry Mumber 4593-17-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,9 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4593-17:
(6*4)+(5*5)+(4*9)+(3*3)+(2*1)+(1*7)=103
103 % 10 = 3
So 4593-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO/c1-7-3-5-9(6-4-7)8(2)10/h7H,3-6H2,1-2H3

4593-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methylpiperidin-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-Acetyl-4-methylpiperidin

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:4593-17-3 SDS

4593-17-3Relevant articles and documents

Cu(II)-Mediated keto C(sp3)-H bond α-acyloxylation of N, N-dialkylamides with aromatic carboxylic acids

Li, Wenjing,Yin, Changzhen,Yang, Xiao,Liu, Hailong,Zheng, Xueli,Yuan, Maolin,Li, Ruixiang,Fu, Haiyan,Chen, Hua

supporting information, p. 7594 - 7599 (2017/09/27)

The selective oxidative coupling of aromatic carboxylic acids with the C(sp3)-H bond adjacent to the keto group of alkylamides has been developed by employing a low cost copper source. This provides an efficient approach for synthesis of O-benzoylglycolamides. The protocol displayed good functional group tolerance. A broad range of benzoic acids directly coupled with alkylamides to afford a variety of O-benzoylglycolamides in moderate to good yields. In addition, a reasonable radical mechanism was proposed based on EPR experiments.

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