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1H-Pyrrole-2-carboxylic acid, 3-ethyl-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138163-73-2

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138163-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138163-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,6 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138163-73:
(8*1)+(7*3)+(6*8)+(5*1)+(4*6)+(3*3)+(2*7)+(1*3)=132
132 % 10 = 2
So 138163-73-2 is a valid CAS Registry Number.

138163-73-2SDS

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 benzyl 3-ethylpyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:138163-73-2 SDS

138163-73-2Downstream Products

138163-73-2Relevant academic research and scientific papers

Porphyrins with exocyclic rings. Part 12. Synthesis of meso,β-butano- and meso,β-pentanoporphyrins from cycloalka[b]pyrroles

Bastian, Jolie A.,Lash, Timothy D.

, p. 6299 - 6310 (2007/10/03)

Pyrroles 5 with b-face fused seven- or eight-membered carbocyclic rings were prepared in good yields by Knorr-type condensations with cycloheptanone or cyclooctanone, respectively. Treatment with lead tetraacetate in dichloromethane afforded the labile ω-acetates 8 and subsequent acid catalyzed condensation with α-unsubstituted pyrrole-2-carboxylates yielded the related pyrrolylcycloalka[b]pyrroles 29 and 30. The α-unsubstituted pyrroles 14 and 23 were prepared by condensing α,β-unsubstituted ketones, or their β-acetoxycarbonyl precursors, with benzyl N-tosylglycinate in the presence of DBU, followed by dehydration with POCl3-pyridine and base catalyzed elimination of p-toluenesulfinic acid. Dipyrrole dibenzyl esters 29 and 30 were hydrogenolysed over 10% Pd-C to give the corresponding dicarboxylic acids. Acid catalyzed condensation with diformyldipyrrylmethane 33 under modified MacDonald '2 + 2' conditions afforded a series of four cycloalkanoporphyrins 4a-d with seven- or eight-membered exocyclic rings. Although the meso,β-butanoporphyrins 4a and 4b were isolated in good yields, poorer results were obtained for the related meso,β-pentanoporphyrin: 4c and 4d. It is proposed that the eight-membered carbocyclic ring distorts the geometry of the open-chain tetrapyrrolic intermediates and this deleterious influence results in the lower yields observed.

An Improved Synthesis of Pyrroles from N-p-Toluenesulfonylglycine Esters and α,β-Unsaturated Aldehydes and Ketones

Lash, Timothy D.,Hoehner, Michael C.

, p. 1671 - 1676 (2007/10/02)

N-p-Toluenesulfonylglycine esters 2 condensed with α,β-unsaturated carbonyl compounds 1 in the presence of the non-nucleophilic base DBU to give hydroxypyrrolidines 3.Dehydration with phosphorous oxychloride-pyridine, followed by DBU mediated elimination

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