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2-Azetidinone,3-methyl-1-(2-propynyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124443-41-0

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124443-41-0 Usage

Chemical Family

Azetidinone

Structure

Contains a five-membered ring with an oxygen and nitrogen atom

Applications

Used in various industrial and pharmaceutical applications

Industrial Use

Employed as a building block in organic synthesis

Pharmaceutical Use

Utilized in the production of pharmaceuticals

Versatility

Its unique chemical structure and properties make it useful in a range of different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 124443-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,4 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124443-41:
(8*1)+(7*2)+(6*4)+(5*4)+(4*4)+(3*3)+(2*4)+(1*1)=100
100 % 10 = 0
So 124443-41-0 is a valid CAS Registry Number.

124443-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-propynyl)-3-methyl-2-azetidinone

1.2 Other means of identification

Product number -
Other names 3-Methyl-1-prop-2-ynyl-azetidin-2-one

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:124443-41-0 SDS

124443-41-0Downstream Products

124443-41-0Relevant academic research and scientific papers

β-Lactam Analogues of Oxotremorine. 3- and 4-Methyl-Substituted 2-Azetidinones

Nilsson, Bjoern M.,Ringdahl, Bjoern,Hacksell, Uli

, p. 580 - 584 (2007/10/02)

Four β-lactam analogues (8-11) of oxotremorine were synthesized and assayed for muscarinic and antimuscarinic activity on the isolated guinea pig ileum.The pharmacological results were compared with those obtained previously with the β-lactam analogue 7 and the 3-, 4-, and 5-methyl-substituted 2-pyrrolidones 2-6.The new compounds were less potent than the corresponding 2-pyrrolidones, regardless of whether they showed agonist (10 and 11), partial agonist (8), or antagonist properties (9) in the ileum assay.The agonists 10 and 11 were about 200-fold less potent than7.Compounds 8-11 also were less potent than the similarly substituted 2-pyrrolidones in inhibiting the binding of the muscarinic antagonist (-)--N-methylscopolamine in homogenates of the rat cerebral cortex.

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