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4-[2-(2-Hydroxy-3,5-dimethylphenyl)-2-oxoethyl]piperidine-2,6-dione is a complex chemical compound featuring a piperidine ring and a diketone moiety. This synthetic compound is characterized by a phenyl group with hydroxy and dimethyl substitutions, along with a ketone functionality attached to the piperidine ring. Its unique structure and properties render it a promising candidate for pharmaceutical applications and as a versatile building block in organic synthesis.

526-02-3

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526-02-3 Usage

Uses

Used in Pharmaceutical Industry:
4-[2-(2-Hydroxy-3,5-dimethylphenyl)-2-oxoethyl]piperidine-2,6-dione is used as a building block for the development of new drugs due to its unique structure and functional groups, which can be utilized in the synthesis of pharmacologically active compounds.
Used in Organic Synthesis:
In the field of organic synthesis, 4-[2-(2-Hydroxy-3,5-dimethylphenyl)-2-oxoethyl]piperidine-2,6-dione serves as a versatile precursor, enabling the creation of a wide range of chemical entities for various applications.

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 academic research and scientific papers

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 actiketal, a glutarimide antibiotic

Kiyota, Hiromasa,Shimizu, Yuko,Oritani, Takayuki

, p. 5887 - 5890 (2007/10/03)

The first synthesis of actiketal (RK-441S), an antibiotic from Streptomyces pulveraceus subsp. epiderstagenes, was achieved from 5,7- dimethylbenzofuran and dimethyl glutaconate via palladium-assisted coupling reaction as a key step. (C) 2000 Elsevier Science Ltd.

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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