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Propan-2-yl {[5-(4-methylphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl}acetate is a complex organic compound with the chemical formula C12H13NO3S. It is a derivative of propan-2-yl acetate, featuring a 1,3,4-oxadiazol-2-yl sulfanyl group attached to the 5-position of a 4-methylphenyl ring. propan-2-yl {[5-(4-methylphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl}acetate is characterized by its unique structure, which includes a five-membered oxadiazole ring fused to a sulfur atom, and a methyl group attached to the phenyl ring. It is likely to be used in the synthesis of various pharmaceuticals or chemical intermediates due to its reactive functional groups and potential for forming stable bonds with other molecules. The compound's properties, such as solubility and reactivity, can be influenced by the presence of the oxadiazole and sulfanyl groups, making it a potentially valuable component in advanced chemical research and development.

5807-40-9

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5807-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5807-40-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5807-40:
(6*5)+(5*8)+(4*0)+(3*7)+(2*4)+(1*0)=99
99 % 10 = 9
So 5807-40-9 is a valid CAS Registry Number.

5807-40-9SDS

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 propan-2-yl 2-[[5-(4-methylphenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetate

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

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More Details:5807-40-9 SDS

5807-40-9Downstream Products

5807-40-9Relevant academic research and scientific papers

Synthesis and certain conversions of 3-(3,3-dichloroallyl)-4-hydroxycoumarin

Avetisyan,Aleksanyan,Alvandzhyan

, p. 39 - 42 (1997)

A method has been developed for the synthesis of 3-(3,3-dichloroalfyl)-4-hydroxycoumarin and 2-thioxo-3-(3,3-dichloroallyl)-4-hydroxy-2H-chromene, and certain conversions of these compounds have been studied. They undergo acid hydrolysis readily, forming (respectively) 3-(4-hydroxy-3-coumarin)- and 3-(2-thioxo-4-hydroxy-2H-chromene-3)propionic acids; these compounds are converted to the corresponding lactones by the action of acetic anhydride. 1997 Plenum Publishing Corporation.

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