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1-phenyl-2-(pyrrol-2'-ylthio)-1-phenylethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93217-56-2

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93217-56-2 Usage

Type of compound

Ketone derivative

Structural features

Contains a phenyl group and a pyrrole ring linked by a thioether bridge

Potential applications

Medicinal chemistry and drug development

Possible pharmacological activities

Exhibits various pharmacological activities

Use as a building block

Can be used for the synthesis of novel pharmaceutical compounds

Opportunities for modification

Presence of the thioether bridge allows for further functionalization and modification

Scientific and industrial relevance

Chemically interesting compound with potential for further exploration in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 93217-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,1 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93217-56:
(7*9)+(6*3)+(5*2)+(4*1)+(3*7)+(2*5)+(1*6)=132
132 % 10 = 2
So 93217-56-2 is a valid CAS Registry Number.

93217-56-2Downstream Products

93217-56-2Relevant academic research and scientific papers

Fused Heterocycles from Pyrrolethiols.Thienopyrroles,Thienopyroles and THiazolopyrroles from Pyrrol-2-yl Phenacyl Sulfides

Harris, Roger L.N.,McFadden, Helen G.

, p. 887 - 892 (2007/10/02)

A reinvestigation of the cyclization of pyrrol-2-yl phenacyl sulfides in polyphosphoric acid has shown that the major product is a thienopyrrole, where rearrangement of the sulfur substituent from position 2 to position 3 has preceded cyclization.W

Fused Heterocycles from Pyrrolethiols

Harris, Roger L. N.,McFadden, Helen G.

, p. 1473 - 1481 (2007/10/02)

Pyrrolethiols are highly reactive bidentate nucleophiles which give a wide variety of fused heterocyclic ring systems on reaction with acylating and alkylating agents via S-substituted intermediates that are in most instances themselves isolable.Represent

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