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3-[3-(dimethylamino)propyl]-2-(3-nitrophenyl)-1,3-thiazolidin-4-one hydrochloride is a complex organic compound with the molecular formula C14H18ClN3O4S. It is a derivative of the thiazolidinone class of compounds, which are known for their diverse range of biological activities, including potential use as antimicrobial, anti-inflammatory, and anticancer agents. The structure of 3-[3-(dimethylamino)propyl]-2-(3-nitrophenyl)-1,3-thiazolidin-4-one hydrochloride features a thiazolidinone ring, a 3-nitrophenyl group, and a dimethylaminopropyl chain, which together contribute to its pharmacological properties. The hydrochloride salt form indicates that it is a salt derived from the reaction of the parent compound with hydrochloric acid, which can improve its solubility and stability. 3-[3-(dimethylamino)propyl]-2-(3-nitrophenyl)-1,3-thiazolidin-4-one hydrochloride is of interest in medicinal chemistry for its potential therapeutic applications, particularly in the development of new drugs targeting various diseases.

5682-67-7

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5682-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5682-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5682-67:
(6*5)+(5*6)+(4*8)+(3*2)+(2*6)+(1*7)=117
117 % 10 = 7
So 5682-67-7 is a valid CAS Registry Number.

5682-67-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[3-(dimethylamino)propyl]-2-(3-nitrophenyl)-1,3-thiazolidin-4-one,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-tert.-Butyl-3-oxo-cyclopenten

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:5682-67-7 SDS

5682-67-7Downstream Products

5682-67-7Relevant academic research and scientific papers

Lone selectivity of the decatungstate-sensitized photooxidation of 1-substituted cycloalkenes

Lykakis, Ioannis N.,Orfanopoulos, Michael

, p. 2131 - 2134 (2007/10/03)

Decatungstate-sensitized oxidation of alkyl and phenyl substituted cycloalkenes in the presence of molecular oxygen shows a general preference for hydrogen abstraction on the congested side of the double bond.

α-Oxidation of ketones using n-cation radicals

Schulz, Manfred,Kluge, Ralph,Sivilai, Li,Kamm, Birgit

, p. 2371 - 2380 (2007/10/02)

Six-membered ring ketones and acyclic ketones were oxidized by stable triarylamminium radical cations in moist acetonitrile at room temperature in the presence of a base to α-hydroxy ketones in good yield. Five-membered ring ketones gave the corresponding αβ-unsaturated compounds.

ON THE SYNTHESIS AND CONFORMATIONAL ASPECTS OF 2-METHYL AND 2-t.BUTYL SUBSTITUTED 1,3-CYCLOPENTANE AND CYCLOHEXANE DIOLS

D'Haenens, L.,Sande, C. C. Van de,Tavernier, D.,Vandewalle, M.

, p. 273 - 282 (2007/10/02)

The diastereomers of 2-methyl-1,3-cyclopentanediol, 2-t.butyl-1,3-cyclopentanediol, 2-methyl-1,3-cyclohexanediol and 2-t.butyl-1,3-cyclohexanediol have been prepared.Configurational assignment and some conformational aspects are described.

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