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116325-48-5

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116325-48-5 Usage

Derivative of indole

Heterocyclic organic compound

Unique chemical properties

Due to the presence of a phenylsulfonyl group on the indole ring

Use in organic synthesis

As a precursor to various pharmaceuticals and agrochemicals

Potential for introducing new functional groups

onto the indole core

Studied for biological activities

Including its role as an inhibitor of certain enzymes

Potential drug candidate

In the treatment of various diseases

Check Digit Verification of cas no

The CAS Registry Mumber 116325-48-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,2 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116325-48:
(8*1)+(7*1)+(6*6)+(5*3)+(4*2)+(3*5)+(2*4)+(1*8)=105
105 % 10 = 5
So 116325-48-5 is a valid CAS Registry Number.

116325-48-5Relevant articles and documents

The generation of Indole-2,3-quinodimethanes from the Deamination of 1,2,3,4-Tetrahydropyrrolo[3,4-b]indoles

Rinderspacher, Alison,Gribble, Gordon W.

, (2020)

A novel generation of indole-2,3-quinodimethanes via the deamination of 1,2,3,4-tetrahydropyrrolo[s3,4-b]indoles is reported.

A Versatile Construction of the 8H-Quinocarbazole Ring System as a Potential DNA Binder

Mohanakrishnan, Arasambattu K.,Srinivasan, Panayencheri C.

, p. 1939 - 1946 (2007/10/02)

A short synthesis of the quino- and quinocarbazoles is repoerted.The key step of the synthesis involves the preparation of suitable 2,3-divinylindoles by consecutive Wittig reactions.The thermal electrocyclic reaction of the divinylindole wi

Synthesis of 3-aryl-5H-pyrido[4,3-b]indoles

Mohanakrishnan,Srinivasan

, p. 2415 - 2424 (2007/10/02)

3-aryl-γ-carbolines (8) were synthesized by the thermal decomposition of 3-azidomethyl-2-(β-arylvinyl)-1-phenylsulfonyl indole (6).

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