Welcome to LookChem.com Sign In|Join Free
  • or
1H-Pyrrole-3,4-dicarboxylic acid, 2,5-bis(trifluoromethyl)-, diethyl ester is a complex organic compound with the chemical formula C11H8F6N2O4. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with one nitrogen atom and four carbon atoms. In this specific compound, the pyrrole ring is substituted with two trifluoromethyl groups at the 2 and 5 positions, and the 3 and4 positions are connected to carboxylic acid groups. These carboxylic acid groups are further esterified with diethyl groups, resulting in the formation of diethyl esters. 1H-Pyrrole-3,4-dicarboxylic acid, 2,5-bis(trifluoromethyl)-, diethyl ester is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and materials science, due to its stability and reactivity.

88149-57-9

Post Buying Request

88149-57-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

88149-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88149-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,4 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88149-57:
(7*8)+(6*8)+(5*1)+(4*4)+(3*9)+(2*5)+(1*7)=169
169 % 10 = 9
So 88149-57-9 is a valid CAS Registry Number.

88149-57-9SDS

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 diethyl 2,5-bis(trifluoromethyl)-1H-pyrrole-3,4-dicarboxylate

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:88149-57-9 SDS

88149-57-9Downstream Products

88149-57-9Relevant academic research and scientific papers

Syntheses and Reactions of 2-Halo-5-thiazolecarboxylates

Lee, Len F.,Schleppnik, Francis M.,Howe, Robert K.

, p. 1621 - 1630 (2007/10/02)

A variety of 2-halo-5-thiazolecarboxylates was prepared from substituted-3-aminoacrylates and 3-ketoesters.Selective reduction of 2-chloro-5-thiazolecarboxylates 4a, 4i and 4j with sodium borohydride in ethanol provided the corresponding 2-halo-5-thiazolemethanols 27 - 29.Nucleophilic displacement on methyl methanesulfonate (32c) occured selectivity at the 5-substituent to provide 2-chloro-4-(trifluoromethyl)-5-(heteroatom-substituted methyl)thiazoles 32d-f.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 88149-57-9