128810-31-1

Basic information

• Product Name: 1H-Indol-5-yl methanesulfonate
• Synonyms: 1H-Indol-5-yl methanesulfonate;1H-INDOL-5-YL METHANESULFONATE(WXG02740)
• CAS NO: 128810-31-1
• Molecular Formula: C₉H₉NO₃S
• Molecular Weight: 211.24
• Mol File: 128810-31-1.mol

Chemical Properties

• Boiling Point: 433.797°C at 760 mmHg
• Flash Point: 216.153°C
• Appearance: /
• Density: 1.438g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.648
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1H-Indol-5-yl methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indol-5-yl methanesulfonate(128810-31-1)
• EPA Substance Registry System: 1H-Indol-5-yl methanesulfonate(128810-31-1)

Safety Data

• Hazardous Substances Data: 128810-31-1(Hazardous Substances Data)

Usage

Chemical class

Indole derivatives

Explanation

1H-Indol-5-yl methanesulfonate belongs to the class of compounds derived from the indole structure.

Explanation

It is a sulfonate ester formed by the condensation of indole with methanesulfonic acid.

Explanation

1H-Indol-5-yl methanesulfonate is used in organic synthesis, aiding in the construction of complex organic molecules.

Explanation

This compound is often used as a reagent in a wide range of chemical reactions due to its versatility.

Explanation

1H-Indol-5-yl methanesulfonate serves as a versatile building block for creating biologically active compounds and pharmaceuticals.

Explanation

The compound is used in the preparation of indole-based molecules for both medicinal and agricultural applications, taking advantage of its unique structure and reactivity.

Explanation

1H-Indol-5-yl methanesulfonate holds significant importance in the fields of organic chemistry and drug discovery due to its wide range of applications and its ability to create complex, biologically active molecules.

Type of compound

Sulfonate ester

Application

Organic synthesis

Use as a reagent

Various chemical reactions

Role in synthesis

Building block for biologically active compounds

Preparation of indole-based molecules

Medicinal and agricultural purposes

Importance in the field

Organic chemistry and drug discovery

InChI:InChI=1/C9H9NO3S/c1-14(11,12)13-8-2-3-9-7(6-8)4-5-10-9/h2-6,10H,1H3

Upstream product

• 1953-54-4 indol-5-ol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 144104-53-0 5-(furan-3-yl)-1H-indole 
• 15861-24-2 1H-indole-5-carbonitrile 
• 267875-62-7 tert-butyl ((1H-indol-5-yl)methyl)carbamate 

Relevant articles and documents

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