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1H-Indole, 5-methyl-2-(phenylmethyl)-, also known as 5-Methyl-2-benzylindole, is an organic compound with the molecular formula C16H15N. It is a derivative of the indole structure, featuring a methyl group at the 5-position and a benzyl group (phenylmethyl) attached to the 2-position. 1H-Indole, 5-methyl-2-(phenylmethyl)- is a white to off-white crystalline solid and is soluble in organic solvents. It is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity. The compound is also known for its potential applications in the development of novel materials and as a building block in the creation of complex organic molecules.

4671-27-6

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4671-27-6 Usage

Molecular Weight

233.30 g/mol The mass of one mole of 1H-Indole, 5-methyl-2-(phenylmethyl)is 233.30 grams.

Structure

1H-Indole, 5-methyl-2-(phenylmethyl)has an indole ring with a methyl group at the 5th position and a phenylmethyl group attached at the 2nd position.

Polarity

Nonpolar The molecule has a relatively even distribution of electronegativity, resulting in a nonpolar character.

Solubility

Insoluble in water Due to its nonpolar character, 1H-Indole, 5-methyl-2-(phenylmethyl)does not dissolve well in water.

Use

Intermediate in synthesis It is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds.

Biological Activity

Potential to interact with biological targets The indole core of the compound gives it the potential to interact with biological targets such as enzymes and receptors, making it a valuable compound in medicinal chemistry research and drug discovery.

Building Block

Important for synthesis of diverse compounds The presence of the phenylmethyl group makes it an important building block for the synthesis of diverse compounds with biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 4671-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4671-27:
(6*4)+(5*6)+(4*7)+(3*1)+(2*2)+(1*7)=96
96 % 10 = 6
So 4671-27-6 is a valid CAS Registry Number.

4671-27-6Downstream Products

4671-27-6Relevant academic research and scientific papers

Ruthenium-catalyzed regioselective synthesis of 2-substituted indoles via ring-opening of epoxides by anilines

Cho, Chan Sik,Kim, Jun Ho,Choi, Heung-Jin,Kim, Tae-Jeong,Shim, Sang Chul

, p. 2975 - 2977 (2003)

Anilines react with epoxides in dioxane at 180°C in the presence of a catalytic amount of a ruthenium catalyst along with tin(II) chloride to afford 2-substituted indoles in moderate to good yields.

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