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2-(Methoxycarbonyl)-5-nitro-1H-pyrrole is a pyrrole derivative with the molecular formula C7H6N2O4. It features a methoxycarbonyl group at the 2-position and a nitro group at the 5-position, giving it a unique chemical structure and reactivity.

13138-73-3

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13138-73-3 Usage

Uses

Used in Pharmaceutical Industry:
2-(Methoxycarbonyl)-5-nitro-1H-pyrrole is used as a building block for the synthesis of various organic molecules and has potential applications in the development of new drugs and other biologically active compounds. Its unique structure and reactivity make it a valuable component in creating novel pharmaceutical agents.
Used in Organic Synthesis:
2-(Methoxycarbonyl)-5-nitro-1H-pyrrole is used as a key intermediate in the synthesis of a wide range of organic molecules. Its versatility in chemical reactions allows for the creation of diverse compounds with various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13138-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,3 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13138-73:
(7*1)+(6*3)+(5*1)+(4*3)+(3*8)+(2*7)+(1*3)=83
83 % 10 = 3
So 13138-73-3 is a valid CAS Registry Number.
InChI:InChI=1S/C6H6N2O4/c1-12-6(9)4-2-3-5(7-4)8(10)11/h2-3,7H,1H3

13138-73-3SDS

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 Methyl 5-nitro-1H-pyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-Nitro-pyrrol-carbonsaeure-2-methylester

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:13138-73-3 SDS

13138-73-3Relevant academic research and scientific papers

New guanidinium-based carboxylate receptors derived from 5-amino-pyrrole-2-carboxylate: Synthesis and first binding studies

Schmuck, Carsten,Dudaczek, Jürgen

, p. 7101 - 7105 (2007/10/03)

The syntheses of two new guanidinium-based carboxylate receptors 2a,b derived from 5-amino pyrrole-2-carboxylate 4 are described. These receptors bind N-acetyl alanine carboxylate and O-acetyl lactate efficiently in aqueous DMSO as could be shown by NMR studies. However, compared to previously reported guanidiniocarbonyl pyrrole receptors 1, the reversal in the direction of the amide group in 2a,b changes both the substrate selectivity (amides are now preferred over esters) and their relative binding affinities. Both effects can be explained based on the calculated complex structure.

Polyaromatic amide compounds and pharmaceutical/cosmetic compositions comprised thereof

-

, (2008/06/13)

Novel pharmaceutically/cosmetically-active polyaromatic amides have the structural formula (I): STR1 wherein Z is a radical --CO--NH-- or --NH--CO--, and are useful for the treatment of a wide variety of disease states, whether human or veterinary, for example dermatological, rheumatic, respiratory, cardiovascular and ophthalmological disorders, as well as for the treatment of mammalian skin and hair conditions/disorders.

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