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1H-Pyrrole-3-carboxylic acid, 4,5-dihydro-4,5-dioxo-2-phenyl-, ethyl ester is a complex organic compound with the chemical formula C12H9NO4. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with one nitrogen atom and four carbon atoms. In this specific compound, the pyrrole ring is modified with a carboxylic acid group at the 3-position, a dihydro-dioxo-phenyl group at the 2-position, and an ethyl ester group attached to the carboxylic acid. This molecule is characterized by its unique structure, which may have potential applications in various fields such as pharmaceuticals, materials science, and chemical research.

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  • 59046-34-3 Structure
  • Basic information

    1. Product Name: 1H-Pyrrole-3-carboxylic acid, 4,5-dihydro-4,5-dioxo-2-phenyl-, ethyl ester
    2. Synonyms:
    3. CAS NO:59046-34-3
    4. Molecular Formula: C13H11NO4
    5. Molecular Weight: 245.235
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 59046-34-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Pyrrole-3-carboxylic acid, 4,5-dihydro-4,5-dioxo-2-phenyl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrrole-3-carboxylic acid, 4,5-dihydro-4,5-dioxo-2-phenyl-, ethyl ester(59046-34-3)
    11. EPA Substance Registry System: 1H-Pyrrole-3-carboxylic acid, 4,5-dihydro-4,5-dioxo-2-phenyl-, ethyl ester(59046-34-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 59046-34-3(Hazardous Substances Data)

59046-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59046-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,4 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59046-34:
(7*5)+(6*9)+(5*0)+(4*4)+(3*6)+(2*3)+(1*4)=133
133 % 10 = 3
So 59046-34-3 is a valid CAS Registry Number.

59046-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethoxycarbonyl-2-phenyl-Δ2-pyrroline-4,5-dione

1.2 Other means of identification

Product number -
Other names 4-ethoxycarbonyl-5-phenyl-1H-pyrrole-2,3-dione

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:59046-34-3 SDS

59046-34-3Relevant articles and documents

Dioxopyrrolines. XXIX. Solvolytic Behavior of 3-Ethoxycarbonyl-2-phenyl-Δ2-pyrroline-4,5-diones in Protic Solvents

Sano, Takehiro,Horiguchi, Yoshie,Tsuda, Yoshisuke

, p. 110 - 120 (2007/10/02)

The solvolytic behavior of 3-ethoxycarbonyl-2-phenyl-Δ2-4,5-diones 7 depends on the N-substituents.On treatment with ethanol or methanol, the NH derivative 7a afforded the corresponding keto ester 9, a product of C5-lactam carbonyl a

Dioxopyrrolines. XXVII. Syntheses of 2-Aryl-3-ethoxycarbonyl-Δ2-pyrroline-4,5-diones

Sano, Takehiro,Horiguchi, Yoshie,Toda, Jun,Imafuku, Kazue,Tsuda, Yoshisuke

, p. 497 - 503 (2007/10/02)

2-Aryl-3-ethoxycarbonyl-Δ2-pyrroline-4,5-diones (3) were easily prepared in good yields by condensation of enamino-esters (2) with oxalyl chloride.The products were characterized by ultraviolet and infrared spectroscopy. Keywords - Δ2-pyrroline-4,5-dione; dioxopyrroline; enamino-ester; ethyl 3-aryl-3-aminopropenoate; 2-aryl-3-ethoxycarbonyl-Δ2-pyrroline-4,5-dione; UV; restricted rotation

FACILE OXY-VINYL SHIFT PROMOTED BY TETRABUTYLAMMONIUM FLUORIDE: A HYDROINDOLE SYNTHESIS

Sano, Takehiro,Toda, Jun,Tsuda, Yoshisuke

, p. 2960 - 2962 (2007/10/02)

The oxy-vinyl alkoxides generated from trimethylsilyloxy-vinyl (or methoxyvinyl)-cyclobutanes by tetra-n-butylammonium fluoride undergo a facile shift to produce a two-carbon unit ring expansion compound under extremely mild conditions.Thus, 7-trimet

2-AZABICYCLOHEPTANE-3,4-DIONES (1). A NOVEL EPIMERIZATION REACTION OF C7-SUBSTITUENTS.

Sano, Takehiro,Horiguchi, Yoshie,Tsuda, Yoshisuke

, p. 355 - 358 (2007/10/02)

On treatment with bases, 7,7-disubstituted and 7-substituted 2-azabicycloheptane-3,4-diones rapidly epimerized at C7 to give a thermodynamically more stable isomer (7-endo isomer in the cases of monosubstituted compounds) predominantly,

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