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100619-73-6

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100619-73-6 Usage

General Description

5-[(Acetyloxy)methyl]-4-ethyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester is a chemical compound with the molecular formula C14H19NO4. It is an ester derivative of pyrrole-2-carboxylic acid, with additional ethyl and acetyloxy methyl groups attached to the pyrrole ring. 5-[(Acetyloxy)methyl]-4-ethyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester is commonly used in organic synthesis and pharmaceutical research, particularly in the development of new drugs and medications. Its specific properties and potential applications depend on its chemical structure, and it may have various biological or pharmacological effects that warrant further investigation. Overall, 5-[(Acetyloxy)methyl]-4-ethyl-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester is a versatile and potentially important chemical compound in the field of chemistry and pharmaceutical science.

Check Digit Verification of cas no

The CAS Registry Mumber 100619-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,1 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100619-73:
(8*1)+(7*0)+(6*0)+(5*6)+(4*1)+(3*9)+(2*7)+(1*3)=86
86 % 10 = 6
So 100619-73-6 is a valid CAS Registry Number.

100619-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-(acetyloxymethyl)-4-ethyl-3-methyl-1H-pyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-acetoxymethyl-4-ethyl-3-methyl-pyrrole-2-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

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

More Details:100619-73-6 SDS

100619-73-6Relevant articles and documents

Syntheses of per-15N labeled etioporphyrins I-IV and a related tetrahydrobenzoporphyrin for applications in organic geochemistry and vibrational spectroscopy

Lash, Timothy D.,Chen, Shaohua

, p. 11577 - 11600 (2007/10/03)

Nitrogen-15 labeled pyrroles have been prepared from commercially available 15N glycine or sodium nitrite using the Barton-Zard, Knorr, and Kleinspehn approaches. These pyrroles were used as intermediates in the synthesis of per-15N labeled porphyrins needed for the analysis and assignment of vibrational spectra for sedimentary porphyrins. Etioporphyrin-I was prepared via pyrromethene intermediates, while etioporphyrins II-V and a related tetrahydrobenzoporphyrin were synthesized via stepwise routes involving the copper(II) mediated cyclization of a,c-biladienes as the key step. Detailed analyses of both the proton and carbon-13 NMR spectra provide nitrogen-15 coupling constants for these important structures.

Thermochemistry of Solution of Linear Pyrroles

Berezin, M. B.,Semeikin, A. S.,V'yugin, A. I.

, p. 1265 - 1268 (2007/10/03)

The enthalpies of solution of a series of symmetrically substituted linear pyrroles in benzene, tetrachloromethane, chloroform, dimethylformamide, and pyridine were measured calorimetrically at 298 K.The effect of substituents in pyrrole molecules on the energy characteristics of their solvation by organic solvents is discussed.

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