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Ethyl 2,5-dioxopyrrole-1-carboxylate (EDPC) is a chemical compound with the molecular formula C8H7NO4 and a molecular weight of 181.14 g/mol. It belongs to the chemical class of pyrroles, which are heterocyclic aromatic organic compounds composed of a five-membered ring with four carbon atoms and one nitrogen atom. EDPC is characterized by its strong, musty odour and a colorless to light yellow appearance. Due to its reactive nature, it is used in various chemical reactions, but it can be hazardous when improperly handled, posing risks to the skin, eyes, and respiratory system. Therefore, it is essential to follow proper handling procedures when using this chemical.

55750-49-7

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55750-49-7 Usage

Uses

Used in Chemical Synthesis:
Ethyl 2,5-dioxopyrrole-1-carboxylate is used as a reactive intermediate for the synthesis of various organic compounds. Its reactivity allows it to participate in a wide range of chemical reactions, making it a valuable component in the preparation of different molecules.
Used in Pharmaceutical Industry:
Ethyl 2,5-dioxopyrrole-1-carboxylate is used as a building block in the development of pharmaceutical compounds. Its unique structure and reactivity enable the creation of new drug candidates with potential therapeutic applications.
Used in Material Science:
Ethyl 2,5-dioxopyrrole-1-carboxylate is used as a component in the synthesis of advanced materials, such as polymers and composites, due to its ability to form stable chemical bonds with other molecules. This contributes to the development of new materials with improved properties for various applications.
Used in Research and Development:
Ethyl 2,5-dioxopyrrole-1-carboxylate is used as a research tool in academic and industrial laboratories. Its unique chemical properties make it an interesting subject for studying reaction mechanisms, exploring new synthetic routes, and discovering novel applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 55750-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,5 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55750-49:
(7*5)+(6*5)+(5*7)+(4*5)+(3*0)+(2*4)+(1*9)=137
137 % 10 = 7
So 55750-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO4/c1-2-12-7(11)8-5(9)3-4-6(8)10/h3-4H,2H2,1H3

55750-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2,5-Dioxopyrrole-1-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 2,5-dioxopyrrole-1-carboxylate

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:55750-49-7 SDS

55750-49-7Relevant articles and documents

Inactivation method

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Page/Page column 16, (2016/05/19)

The present invention relates to the field of thermostable enzymes, methods for their inactivation, and related uses, kits and reagents. In particular, the invention relates to a method for reversible inactivation of thermophilic enzymes by chemical modification under aqueous or non-aqueous conditions.

Indium-Catalyzed Amide Allylation of N-Carbonyl Imides: Formation of Azaspiro-γ-lactones via Ring Opening-Reclosure

Sengoku, Tetsuya,Murata, Yusuke,Aso, Yuwa,Kawakami, Ai,Inuzuka, Toshiyasu,Sakamoto, Masami,Takahashi, Masaki,Yoda, Hidemi

supporting information, p. 5846 - 5849 (2015/12/11)

A novel and facile synthesis of azaspiro-γ-lactones with a methylene-lactam framework from N-carbonyl imides is described. Mechanistic investigations provide evidence for a two-step reaction process involving ZnCl2-promoted addition of β-amido allylindium species followed by an unexpectedly molecular-sieves-mediated ring opening-reclosure concomitantly with the loss of an N-carbonyl unit.

Dendrimer-like polymeric DNAs as chemiluminescence probes for amplified detection of telomere DNA on a solid-phase membrane

El-Mahdy, Ahmed F. M.,Shibata, Takayuki,Kabashima, Tsutomu,Kai, Masaaki

supporting information, p. 859 - 861 (2014/01/06)

For the first time, an amplified chemiluminescence (CL) detection of the telomere DNA spotted on a nylon membrane is described here, based on the direct hybridization with the CL probe of dendrimer-like polymeric DNAs possessing a large number of guanine moieties. This probe was synthesized by sense and antisense hybridization between Y-shaped DNAs and then could hybridize with the target DNA. The Royal Society of Chemistry.

Novel compositions magnetic particles covered with gem-bisphosphonate derivatives

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, (2010/12/29)

The invention relates to a composition comprising acid magnetic particles (p) based on an iron compound, the acid magnetic particles (p) being complexed by one or more gem-bisphosphonate compounds, of formula I: [in-line-formulae]X-L-CH(PO3H2)2 ??(I)[/in-line-formulae]in which: L represents an organic group connecting the X group to the gem-bisphosphonate group —CH(PO3H2)2;X represents a chemical group capable of reacting with a biovector; all or some of the X groups of the particles optionally being coupled to a biovector. The invention relates also to a process for the preparation of the compositions and their use, in particular as contrast products for Magnetic Resonance Imaging (MRI).

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