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54530-04-0

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54530-04-0 Usage

General Description

(CIS/TRANS)-2,5-DIMETHYL-1-N-(4'-METHYL)PHENYLPYRROLIDINE is a chemical compound belonging to the pyrrolidine class. It is a derivative of pyrrolidine with a cis/trans isomer. (CIS/TRANS)-2,5-DIMETHYL-1-N-(4'-METHYL)PHENYLPYRROLIDINE contains a pyrrolidine ring with two methyl groups at positions 2 and 5, and a 4'-methylphenyl group attached to the nitrogen atom. It is commonly used in organic synthesis for the construction of complex organic molecules and pharmaceutical compounds. The specific properties and applications of this compound may vary depending on the isomeric form and the context in which it is used.

Check Digit Verification of cas no

The CAS Registry Mumber 54530-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54530-04:
(7*5)+(6*4)+(5*5)+(4*3)+(3*0)+(2*0)+(1*4)=100
100 % 10 = 0
So 54530-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H19N/c1-10-4-8-13(9-5-10)14-11(2)6-7-12(14)3/h4-5,8-9,11-12H,6-7H2,1-3H3

54530-04-0SDS

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 2,5-dimethyl-1-(4-methylphenyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names 2,5-Dimethyl-1-N-(4'-Methyl)Phenylpyrrolidine

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:54530-04-0 SDS

54530-04-0Relevant articles and documents

Cyclodextrin-based PNN supramolecular assemblies: a new class of pincer-type ligands for aqueous organometallic catalysis

Menuel,Bertaut,Monflier,Hapiot

, p. 13504 - 13512 (2015/08/03)

Water-soluble cyclodextrins (CDs) bearing two nitrogen atoms as metal coordinating sites have been synthesized. An appropriate phosphane could be included within their cavity through the primary face to form self-assembled PNN supramolecular edifices. Once the PNN ligands were coordinated to platinum, the resulting complexes proved to be very effective as catalysts in a domino reaction, where a Pt-catalyzed reduction of nitrobenzene was followed by a Paal-Knorr pyrrole reaction. In the nitrobenzene reduction, the modified CDs acted both as first- and second-sphere ligands. Contrary to an acyclic glucopyranose-based NN ligand unable to interact with a phosphane ligand, the CD-based PNN ligands stabilized the catalytic species in water by supramolecular means. Interestingly, the product and the water-soluble Pt-catalyst could be recovered in two different phases once the reaction was complete.

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