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1001070-29-6

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1001070-29-6 Usage

Structure

Pyrrolopyridine derivative with a fluorine atom at the 6 position and a phenylsulfonyl group attached at the 1 position

Potential pharmaceutical applications

Ability to interact with biological targets such as enzymes or receptors

Physicochemical properties

Presence of the fluorine atom and the sulfonyl group may impart specific properties that may be useful in drug development or medicinal chemistry research

Need for further studies

To fully understand the potential uses and properties of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 1001070-29-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,0,7 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1001070-29:
(9*1)+(8*0)+(7*0)+(6*1)+(5*0)+(4*7)+(3*0)+(2*2)+(1*9)=56
56 % 10 = 6
So 1001070-29-6 is a valid CAS Registry Number.

1001070-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfonyl)-6-fluoropyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 1H-Pyrrolo[2,3-b]pyridine,6-fluoro-1-(phenylsulfonyl)

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:1001070-29-6 SDS

1001070-29-6Downstream Products

1001070-29-6Relevant articles and documents

7-Azaindole derivatives as potential partial nicotinic agonists

Stoit, Axel R.,den Hartog, Arnold P.,Mons, Harry,van Schaik, Sjoerd,Barkhuijsen, Nynke,Stroomer, Cees,Coolen, Hein K.A.C.,Reinders, Jan Hendrik,Adolfs, Tiny J.P.,van der Neut, Martina,Keizer, Hiskias,Kruse, Chris G.

, p. 188 - 193 (2008/12/23)

We have investigated a series of 7-azaindoles as potential partial agonists of the α4β2 nicotinic acetylcholine receptor (nAChR). Three series of 7-azaindole derivatives have been synthesized and evaluated for rat brain neuronal nicotinic receptor affinity and functional activity. Compound (+)-51 exhibited the most potent nAChR binding (Ki = 10 nM). Compound 30A demonstrated both moderate binding affinity and partial agonist potency, thus representing a promising lead for the indications of cognition and smoking cessation.

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