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1125702-76-2

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1125702-76-2 Usage

Type of compound

Ketone derivative

Cyclobutyl group

A four-membered carbon ring

Pyridine ring

A six-membered nitrogen-containing aromatic ring

Common uses

Building block in organic synthesis
Building block in medicinal chemistry
Production of pharmaceuticals and agrochemicals

Potential applications

Ligand in coordination chemistry
Materials science
Catalysis

Pharmacological properties

Studied for potential therapeutic use in various diseases

Check Digit Verification of cas no

The CAS Registry Mumber 1125702-76-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,5,7,0 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1125702-76:
(9*1)+(8*1)+(7*2)+(6*5)+(5*7)+(4*0)+(3*2)+(2*7)+(1*6)=122
122 % 10 = 2
So 1125702-76-2 is a valid CAS Registry Number.

1125702-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclobutyl-2-pyridin-2-ylethanone

1.2 Other means of identification

Product number -
Other names 1-cyclobutyl-2-(pyridin-2-yl)ethanone

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:1125702-76-2 SDS

1125702-76-2Downstream Products

1125702-76-2Relevant articles and documents

Synthesis of functionalised 4H-quinolizin-4-ones via tandem Horner-Wadsworth-Emmons olefination/cyclisation

Muir, Calum W.,Kennedy, Alan R.,Redmond, Joanna M.,Watson, Allan J. B.

, p. 3337 - 3340 (2013/06/05)

4H-Quinolizin-4-ones are a unique class of heterocycle with valuable physicochemical properties and which are emerging as key pharmacophores for a range of biological targets. A tandem Horner-Wadsworth-Emmons olefination/cyclisation method has been developed to allow facile access to substituted 4H-quinolizin-4-ones encoded with a range of functional groups.

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