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dimethyl 2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40801-09-0

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40801-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40801-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40801-09:
(7*4)+(6*0)+(5*8)+(4*0)+(3*1)+(2*0)+(1*9)=80
80 % 10 = 0
So 40801-09-0 is a valid CAS Registry Number.

40801-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2,5-dimethyl-1H-pyrrole-3,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names dimethyl 2,5-dimethyl-pyrrole-3,4-dicarboxylate

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:40801-09-0 SDS

40801-09-0Downstream Products

40801-09-0Relevant academic research and scientific papers

Trifluoroethanol as a Unique Additive for the Chemoselective Electrooxidation of Enamines to Access Unsymmetrically Substituted NH-Pyrroles

Baidya, Mrinmay,De Sarkar, Suman,Maiti, Debabrata,Roy, Lisa

supporting information, (2021/12/23)

An electrochemical method for the synthesis of unsymmetrically substituted NH-pyrroles is described. The synthetic strategy comprises a challenging heterocoupling between two structurally diverse enamines via sequential chemoselective oxidation, addition,

Reactivity of a new alkenyl phenyliodonium tosylate derived from methyl 3-aminocrotonate

Papoutsis, Ioannis,Spyroudis, Spyros,Varvoglis, Anastasios

, p. 1005 - 1012 (2007/10/03)

Methyl 3-aminocrotonate reacts with [hydroxy(tosyloxy)iodo]benzene to afford the corresponding E-2-phenyliodonio tosylate in good yield. This new alkenyl iodonium sat upon reaction with various nucleophiles offers an easy access to substituted enamine der

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