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51856-25-8

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51856-25-8 Usage

General Description

6H-thieno[2,3-b]pyrrole-5-carboxylic acid is a chemical compound with a unique structure that consists of a thieno[2,3-b]pyrrole ring fused to a carboxylic acid group at the 5-position. 6H-Thieno[2,3-b]pyrrole-5-carboxylic acid is a heterocyclic organic molecule that can be used in various organic synthesis reactions and medicinal chemistry research. Its structure and reactivity make it a potential building block for the synthesis of complex organic molecules and pharmaceutical compounds. The carboxylic acid functionality also enables the compound to participate in important chemical reactions such as esterification and amidation, expanding its synthetic utility. Additionally, its potential biological activity makes it an interesting target for drug discovery and development. Overall, 6H-thieno[2,3-b]pyrrole-5-carboxylic acid is a versatile chemical compound with potential applications in both organic synthesis and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 51856-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51856-25:
(7*5)+(6*1)+(5*8)+(4*5)+(3*6)+(2*2)+(1*5)=128
128 % 10 = 8
So 51856-25-8 is a valid CAS Registry Number.

51856-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6H-THIENO[2,3-B]PYRROLE-5-CARBOXYLIC ACID

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:51856-25-8 SDS

51856-25-8Downstream Products

51856-25-8Relevant articles and documents

FLUORESCENT COMPOUND AND LABELING AGENT COMPRISING THE SAME

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Page/Page column 18; 19, (2009/03/07)

A novel fluorescent compound having a high light fastness, high fluorescence quantum yield and sharp absorption spectrum, which emits fluorescence having a wavelength in long wavelength region, as well as its use as a labeling agent, is disclosed. In Form

The discovery of fused pyrrole carboxylic acids as novel, potent d-amino acid oxidase (DAO) inhibitors

Sparey, Tim,Abeywickrema, Pravien,Almond, Sarah,Brandon, Nick,Byrne, Noel,Campbell, Alister,Hutson, Pete H.,Jacobson, Marlene,Jones, Brian,Munshi, Sanjeev,Pascarella, Danette,Pike, Andrew,Prasad, G. Sridhar,Sachs, Nancy,Sakatis, Melanie,Sardana, Vinod,Venkatraman, Shankar,Young, Mary Beth

scheme or table, p. 3386 - 3391 (2009/04/06)

The 'NMDA hypofunction hypothesis of schizophrenia' can be tested in a number of ways. DAO is the enzyme primarily responsible for the metabolism of d-serine, a co-agonist for the NMDA receptor. We identified novel DAO inhibitors, in particular, acid 1, which demonstrated moderate potency for DAO in vitro and ex vivo, and raised plasma d-serine levels after dosing ip to rats. In parallel, analogues were prepared to survey the SARs of 1.

Novel thienopyrrole glycogen phosphorylase inhibitors: Synthesis, in vitro SAR and crystallographic studies

Whittamore, Paul R.O.,Addie, Matthew S.,Bennett, Stuart N.L.,Birch, Alan M.,Butters, Michael,Godfrey, Linda,Kenny, Peter W.,Morley, Andrew D.,Murray, Paul M.,Oikonomakos, Nikos G.,Otterbein, Ludovic R.,Pannifer, Andrew D.,Parker, Jeremy S.,Readman, Kristy,Siedlecki, Pawel S.,Schofield, Paul,Stocker, Andy,Taylor, Melvyn J.,Townsend, Linda A.,Whalley, David P.,Whitehouse, Jennifer

, p. 5567 - 5571 (2007/10/03)

Two series of novel thienopyrrole inhibitors of recombinant human liver glycogen phosphorylase a (GPa) which are effective in reducing glucose output from rat hepatocytes are described. Representative compounds have been shown to bind at the dimer interface site of the rabbit muscle enzyme by X-ray crystallography.

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