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2543-57-9

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2543-57-9 Usage

Uses

4-(dimethylamino)-2-Butanone is a useful building block extracted from volatile oil in Semen persicae-Flos carthami. 4-(dimethylamino)-2-Butanone is used as a component of lubricating oil used to improve the viscosity index and sludge dispersion properties of hydrogenated lithiated copolymers.

Check Digit Verification of cas no

The CAS Registry Mumber 2543-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,4 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2543-57:
(6*2)+(5*5)+(4*4)+(3*3)+(2*5)+(1*7)=79
79 % 10 = 9
So 2543-57-9 is a valid CAS Registry Number.

2543-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Dimethylamino)butan-2-one

1.2 Other means of identification

Product number -
Other names 2-Butanone,4-(dimethylamino)-(6CI,7CI,8CI,9CI)

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:2543-57-9 SDS

2543-57-9Relevant articles and documents

Chemical and biological profile of racemic and optically active dialkylaminoalkylnaphthalenes with analgesic activity

Azzolina, Ornella,Collina, Simona,Brusotti, Gloria,Rossi, Daniela,Callegari, Athos,Linati, Laura,Barbieri, Annalisa,Ghislandi, Victor

, p. 1073 - 1081 (2002)

The racemic mixtures and the enantiomers of dialkylaminoalkylnaphthalenes are described here as novel analgesic agents with potencies similar, or superior to that of morphine. The synthesis and isolation of the pure enantiomers and a study of the absolute

Gaining in pan-affinity towards sigma 1 and sigma 2 receptors. SAR studies on arylalkylamines

Rossi, Daniela,Rui, Marta,Di Giacomo, Marcello,Schepmann, Dirk,Wünsch, Bernhard,Monteleone, Stefania,Liedl, Klaus R.,Collina, Simona

, p. 11 - 19 (2016/12/22)

Sigma Receptor (SR) modulators are involved in different signal transduction pathways, representing important pharmacological/therapeutic tools in several pathological conditions, such as neurodegenerative diseases and cancers. To this purpose, numerous c

Identification of a potent and selective ρ1 receptor agonist potentiating NGF-induced neurite outgrowth in PC12 cells

Rossi, Daniela,Pedrali, Alice,Urbano, Mariangela,Gaggeri, Raffaella,Serra, Massimo,Fernández, Leyden,Fernández, Michael,Caballero, Julio,Ronsisvalle, Simone,Prezzavento, Orazio,Schepmann, Dirk,Wuensch, Bernhard,Peviani, Marco,Curti, Daniela,Azzolina, Ornella,Collina, Simona

scheme or table, p. 6210 - 6224 (2011/12/02)

Herein we report the synthesis, drug-likeness evaluation, and in vitro studies of new sigma (ρ) ligands based on arylalkenylaminic scaffold. For the most active olefin the corresponding arylalkylamine was studied. Novel arylalkenylamines generally possess

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