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METHYL 2,5-DIMETHYL-4-ETHYLPYRROLE-3-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27093-38-5

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27093-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27093-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,9 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27093-38:
(7*2)+(6*7)+(5*0)+(4*9)+(3*3)+(2*3)+(1*8)=115
115 % 10 = 5
So 27093-38-5 is a valid CAS Registry Number.

27093-38-5SDS

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 methyl 4-ethyl-2,5-dimethyl-1H-pyrrole-3-carboxylate

1.2 Other means of identification

Product number -
Other names METHYL 2,5-DIMETHYL-4-ETHYLPYRROLE-3-CARBOXYLATE

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:27093-38-5 SDS

27093-38-5Downstream Products

27093-38-5Relevant academic research and scientific papers

Transaminase-Mediated Amine Borrowing via Shuttle Biocatalysis

O'Reilly, Elaine,O'Sullivan, Rachel,Ryan, James,Taday, Freya

supporting information, (2022/01/04)

Shuttle catalysis has emerged as a useful methodology for the reversible transfer of small functional groups, such as CO and HCN, and goes far beyond transfer hydrogenation chemistry. While a biocatalytic hydrogen-borrowing methodology is well established, the biocatalytic borrowing of alternative functional groups has not yet been realized. Herein, we present a new concept of amine borrowing via biocatalytic shuttle catalysis, which has no counterpart in chemo-shuttle catalysis and allows efficient intermolecular amine shuttling to generate reactive intermediates in situ. By coupling this dynamic exchange with an irreversible downstream step to displace the reaction equilibrium in the forward direction, high conversion to target products can be achieved. We showcase the potential of this amine-borrowing methodology using a biocatalytic equivalent of both the Knorr-pyrrole synthesis and Pictet-Spengler reaction.

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