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293325-90-3

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293325-90-3 Usage

Molecular structure

1H-Indole, 1-(triphenylmethyl)-, consists of an indole ring with a triphenylmethyl group attached at the 1 position.

Usage

It is commonly used in organic synthesis as a versatile building block for creating various biologically active compounds, such as pharmaceuticals and agrochemicals.

Medicinal properties

Benzhydryl indole has been found to possess anti-inflammatory, anti-cancer, and antimicrobial properties, making it a valuable compound in medicinal chemistry research.

Unique structure and reactivity

Its unique structure and reactivity make it a useful intermediate for creating diverse and complex molecules with potential pharmacological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 293325-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,3,2 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 293325-90:
(8*2)+(7*9)+(6*3)+(5*3)+(4*2)+(3*5)+(2*9)+(1*0)=153
153 % 10 = 3
So 293325-90-3 is a valid CAS Registry Number.

293325-90-3Downstream Products

293325-90-3Relevant articles and documents

A simple synthetic protocol for the protection of amides, lactams, ureas, and carbamates

Reddy, Dandu R,Iqbal, Mohamed A,Hudkins, Robert L,Messina-McLaughlin, Patricia A,Mallamo, John P

, p. 8063 - 8066 (2007/10/03)

A new procedure for protecting the amide, lactam, urea, and carbamate NH group with a triphenylmethyl (Tr) group is described. The utility of this method is illustrated with molecules that contain other functional groups. A mild deprotection using trifluoroacetic acid makes this a useful method for attaching amide groups on resin for combinatorial synthesis.

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