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1H-Pyrrole-3-carboxylic acid, 4-amino-2-methyl-5-phenyl, ethyl ester is a complex organic compound with the chemical formula C16H18N2O2. It is a derivative of pyrrole-3-carboxylic acid, featuring an amino group at the 4-position, a methyl group at the 2-position, and a phenyl group at the 5-position. The ethyl ester functional group is attached to the carboxylic acid, indicating that it is an ester derivative. 1H-Pyrrole-3-carboxylic acid, 4-amino-2-methyl-5-phenyl-, ethyl ester is characterized by its unique molecular structure, which contributes to its specific chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. The compound's name provides a detailed description of its structure, highlighting the presence of a pyrrole ring, the substitution pattern of the amino, methyl, and phenyl groups, and the ethyl ester group.

59133-02-7

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59133-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59133-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,3 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59133-02:
(7*5)+(6*9)+(5*1)+(4*3)+(3*3)+(2*0)+(1*2)=117
117 % 10 = 7
So 59133-02-7 is a valid CAS Registry Number.

59133-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-amino-2-methyl-5-phenylpyrrol-3-yl-carboxylate

1.2 Other means of identification

Product number -
Other names 4-amino-2-methyl-5-phenyl-pyrrole-3-carboxylic acid ethyl ester

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:59133-02-7 SDS

59133-02-7Relevant academic research and scientific papers

PYRROLE STUDIES. PART 35. AERIAL OXIDATION OF 4-SUBSTITUTED 3-AMINO-2,5-DIMETHYLPYRROLES. AN X-RAY CRYSTALLOGRAPHIC AND SPECTROSCOPIC STUDY OF THE OXIDATION PRODUCTS

Cirrincione, Girolamo,Dattolo, Gaetano,Almerico, Anna Maria,Aiello, Enrico,Jones R.Alan,et all

, p. 1959 - 1962 (2007/10/02)

The attempted preparation of ethyl 3-amino-2,5-dimethylpyrrole-4-carboxylate and 4-acetyl-3-amino-2,5-dimethylpyrrole by standard ring synthesis procedures reculted in the exclusive isolation of 2-hydroxy-2H-pyrroles, as indicated by 1H and 13C n.m.r.spec

THE METHYLENE BLUE-SENSITIZED PHOTO-OXIDATION OF SOME 3-ACYL- AND 3-ALKOXYCARBONYL-4-AMINO-2-METHYL-5-PHENYLPYRROLES

Tarzia, Giorgio,Panzone, Gianbattista,Ripamonti, Ambrogio

, p. 261 - 266 (2007/10/02)

The methylene blue-sensitized photo-oxidation of some 3-acyl- and 3-alkoxycarbonyl-4-amino-2-methyl-5-phenylpyrroles yields compounds derivable from the decomposition of 5-hydroperoxides or 4,5-dioxetanes, depending on the substitution pattern of the 4-am

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