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1263987-17-2

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  • 1-[tert-butyl(dimethyl)silyl]-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

    Cas No: 1263987-17-2

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1263987-17-2 Usage

Chemical structure

1-(tert-Butyldimethylsilyl)-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole is a complex chemical compound with an indole ring, a tert-butyldimethylsilyl group, and a 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl group attached to it.

Indole ring

The core structure of the compound is an indole ring, which is a bicyclic organic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

tert-Butyldimethylsilyl group

This group is attached to the indole ring and consists of a silicon atom bonded to three methyl groups and a tert-butyl group. It provides steric bulk and can protect the indole ring during chemical reactions.

4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl group

This group is attached to the indole ring and consists of a boron atom bonded to two oxygen atoms and two carbon atoms, each of which is bonded to three methyl groups. This group can participate in Suzuki-Miyaura cross-coupling reactions, making the compound a useful building block for more complex molecules.

Application in organic synthesis

The compound is often used as a building block in organic synthesis due to its unique structure and reactivity.

Use in medicinal chemistry, pharmaceuticals, and materials science

The compound's properties make it a valuable tool for chemists working in these fields, as it can be used to create more complex molecules with potential applications in drug development and material design.

Suzuki-Miyaura cross-coupling reactivity

The 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl group in the compound allows it to participate in Suzuki-Miyaura cross-coupling reactions, which are widely used in the synthesis of complex organic molecules, including pharmaceuticals and bioactive compounds.

Steric bulk from the tert-butyldimethylsilyl group

The presence of the bulky tert-butyldimethylsilyl group can protect the indole ring during chemical reactions, making it a useful protecting group in synthetic sequences.

Potential for further functionalization

The compound's structure allows for further functionalization and modification, enabling the synthesis of a wide range of complex molecules with diverse properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1263987-17-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,9,8 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1263987-17:
(9*1)+(8*2)+(7*6)+(6*3)+(5*9)+(4*8)+(3*7)+(2*1)+(1*7)=192
192 % 10 = 2
So 1263987-17-2 is a valid CAS Registry Number.

1263987-17-2Upstream product

1263987-17-2Downstream Products

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