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526-02-3

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526-02-3 Usage

General Description

4-[2-(2-Hydroxy-3,5-dimethylphenyl)-2-oxoethyl]piperidine-2,6-dione is a chemical compound with a complex structure consisting of a piperidine ring and a diketone moiety. It is a synthetic compound that has potential pharmaceutical applications due to its unique structure and properties. The compound contains a phenyl group substituted with hydroxy and dimethyl groups, as well as a piperidine ring with a ketone functionality attached. 4-[2-(2-Hydroxy-3,5-dimethylphenyl)-2-oxoethyl]piperidine-2,6-dione can be used as a building block in organic synthesis or as a precursor for the development of new drugs. The functional groups present in this compound make it a versatile starting material for the synthesis of various pharmacologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 526-02-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 526-02:
(5*5)+(4*2)+(3*6)+(2*0)+(1*2)=53
53 % 10 = 3
So 526-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO4/c1-8-3-9(2)15(20)11(4-8)12(17)5-10-6-13(18)16-14(19)7-10/h3-4,10,20H,5-7H2,1-2H3,(H,16,18,19)

526-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-Hydroxy-3,5-dimethylphenacyl)glutarimide

1.2 Other means of identification

Product number -
Other names 4-[2-(2-Hydroxy-3,5-dimethylphenyl)-2-oxoethyl]piperidine-2,6-dione

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:526-02-3 SDS

526-02-3Relevant articles and documents

Synthesis and antiviral activities of synthetic glutarimide derivatives

Ji, Xing-Yue,Zhong, Zhao-Jin,Xue, Si-Tu,Meng, Shuai,He, Wei-Ying,Gao, Rong-Mei,Li, Yu-Huan,Li, Zhuo-Rong

experimental part, p. 1436 - 1441 (2010/12/25)

A series of novel glutarimide compounds were synthesized and their antiviral activities were evaluated. The compounds displaying the strongest antiviral activities included 5, 6f, 7e and 9 against coxsackievirus B3 (Cox B3), 10 and 6f against influenza vi

SYNTHESIS OF ACTIPHENOL AND ITS NORMETHYL ANALOGUES AND 6-HYDROXY DERIVATIVES

Lakhvich, F. A.,Buravskaya, T. N.,Akhrem, A. A.

, p. 526 - 529 (2007/10/02)

The synthesis has been achieved of the natural antibiotic actiphenol and its 4,6-bisnormethyl and 4,5-bisnormethyl-5-methyl analogues and also its 6-hydroxy derivatives, starting from 2-(β-glutarimidyl-acetyl)cyclohexane-1,3-diones.

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