CAS 3260-63-7

1H-Indol-3-ol, 1-methyl-, 3-acetate

Description:

1H-Indol-3-ol, 1-methyl-, 3-acetate, with the CAS number 3260-63-7, is an organic compound belonging to the indole family. It features a methyl group and an acetate functional group attached to the indole structure, which is a bicyclic compound composed of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This compound is typically characterized by its aromatic properties, which contribute to its stability and reactivity. It is often used in various chemical syntheses and may exhibit biological activity, making it of interest in pharmaceutical research. The presence of the acetate group suggests it may participate in esterification reactions or hydrolysis, influencing its solubility and reactivity in different solvents. Additionally, the indole structure is known for its role in many natural products and biological systems, including neurotransmitters and hormones. Overall, 1H-Indol-3-ol, 1-methyl-, 3-acetate is a versatile compound with potential applications in medicinal chemistry and organic synthesis.

Formula: C₁₁H₁₁NO₂

InChI: InChI=1S/C11H11NO2/c1-8(13)14-11-7-12(2)10-6-4-3-5-9(10)11/h3-7H,1-2H3

InChI key: InChIKey=QSVQMVRTWNDRDT-UHFFFAOYSA-N

SMILES: O(C(C)=O)C=1C=2C(N(C)C1)=CC=CC2

Synonyms:

• (1-Methylindol-3-yl) acetate
• 1-methyl-1H-indol-3-yl acetate
• 1H-Indol-3-ol, 1-methyl-, 3-acetate
• 1H-Indol-3-ol, 1-methyl-, acetate (ester)
• 3-Acetoxy-1-methylindole
• Indol-3-ol, 1-methyl-, acetate
• Indol-3-ol, 1-methyl-, acetate (ester)
• Indoxyl, 1-methyl-, acetate
• N-Methylindoxyl acetate

N-Methylindoxyl acetate

CAS: 3260-63-7

Formula: C₁₁H₁₁NO₂

Purity: 95%

Molecular weight: 189.2105

Ref: IN-DA00CASJ

N-Methylindoxyl acetate

CAS: 3260-63-7

N-Methylindoxyl acetate

Purity: 95%

Molecular weight: 189.21g/mol

Ref: 54-BIM0149

N-Methylindolyl-3-acetate

Controlled Product

CAS: 3260-63-7

N-Methylindolyl-3-acetate is a serine protease inhibitor that binds to the active site serine of butyrylcholinesterase. It is used in clinical settings as an antidote for organophosphate poisoning. N-Methylindolyl-3-acetate binds to the active site serine of butyrylcholinesterase, which is essential for the hydrolysis of choline esters. The binding prevents substrate binding, thereby stabilizing and slowing down the rate of hydrolysis. This drug also slows down the rate of reaction by increasing the hydration level around it, which subsequently increases its kinetic and decreases its hydration. The substrate concentration also plays a role in how quickly a reaction will occur because there needs to be enough substrate molecules for it to work on.

Formula: C₁₁H₁₁NO₂

Purity: Min. 95%

Molecular weight: 189.21 g/mol

Ref: 3D-FM35461