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1-Pyrrolidinecarboxylic acid, 2,5-dioxo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25543-13-9

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25543-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25543-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,4 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25543-13:
(7*2)+(6*5)+(5*5)+(4*4)+(3*3)+(2*1)+(1*3)=99
99 % 10 = 9
So 25543-13-9 is a valid CAS Registry Number.

25543-13-9SDS

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 methyl 2,5-dioxopyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-(Methoxycarbonyl)-2,5-pyrrolidindion

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:25543-13-9 SDS

25543-13-9Downstream Products

25543-13-9Relevant academic research and scientific papers

Hydrogenations without hydrogen: Titania photocatalyzed reductions of maleimides and aldehydes

Manley, David W.,Buzzetti, Luca,MacKessack-Leitch, Andrew,Walton, John C.

, p. 15324 - 15338 (2015/01/16)

A mild procedure for the reduction of electron-deficient alkenes and carbonyl compounds is described. UVA irradiations of substituted maleimides with dispersions of titania (Aeroxide P25) in methanol/acetonitrile (1:9) solvent under dry anoxic conditions led to hydrogenation and production of the corresponding succinimides. Aromatic and heteroaromatic aldehydes were reduced to primary alcohols in similar titania photocatalyzed reactions. A mechanism is proposed which involves two proton-coupled electron transfers to the substrates at the titania surface.

A convenient one-pot synthesis of polysubstituted pyrroles from N-protected succinimides

Kobeissi, Marwan,Yazbeck, Ogaritte,Chreim, Yamama

supporting information, p. 2523 - 2526 (2014/05/06)

The dienamine products formed by the reaction between polysubstituted succinimides and the Petasis reagent were subjected to isomerization under mild acidic conditions to give polysubstituted pyrroles in excellent yields (85-95%). The scope and limitations of this methodology are explored.

Unconventional titania photocatalysis: Direct deployment of carboxylic acids in alkylations and annulations

Manley, David W.,McBurney, Roy T.,Miller, Phillip,Howe, Russell F.,Rhydderch, Shona,Walton, John C.

supporting information; experimental part, p. 13580 - 13583 (2012/10/08)

Under dry, anaerobic conditions, TiO2 photocatalysis of carboxylic acid precursors resulted in carbon-carbon bond-forming processes. High yields of dimers were obtained from TiO2 treatment of carboxylic acids alone. On inclusion of electron-deficient alkenes, efficient alkylations were achieved with methoxymethyl and phenoxymethyl radicals. In reactions with maleic anhydride or maleimides, phenoxyacetic acid produced chromenedione derivatives in addition to adducts. These photocatalytic reactions are simple and cheap to perform, and the TiO2 is easily removed by filtration. The anaerobic photocatalysis strategy offers a range of synthetic possibilities.

RENIN INHIBITORS IV

-

, (2008/06/13)

The invention concerns novel renin-inhibitory peptides which are useful for treating renin-assocated hypertension, hyperaldosteronism, and congestive heart failure. Processes for preparing the peptides, compositions containing them and methods of using them are included. Also included is a diagnostic method which uses the compounds to determine the presence of renin-associated hypertension or hyperaldosteronism.

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