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3-(1-[(4-Methylphenyl)sulfonyl]-1H-indol-3-yl)acrylic acid, also known as MSIA, is a chemical compound characterized by the presence of a sulfonyl group, an indole ring, and an acrylic acid group. MSIA is recognized for its potential therapeutic properties and is widely utilized in pharmaceutical research and drug discovery. Its unique structure and reactivity contribute to its value as a starting material for synthesizing various bioactive molecules, while also serving as a building block in organic synthesis for creating complex organic molecules with distinctive functional groups.

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  • 298187-97-0 Structure
  • Basic information

    1. Product Name: 3-(1-[(4-METHYLPHENYL)SULFONYL]-1H-INDOL-3-YL)ACRYLIC ACID
    2. Synonyms: RARECHEM AL BK 0453;3-(1-[(4-METHYLPHENYL)SULFONYL]-1H-INDOL-3-YL)ACRYLIC ACID;3-{1-[(4-methylphenyl)sulphonyl]-1H-indol-3-yl}acrylic acid;3-{1-[(4-Methylphenyl)sulphonyl]-1H-indol-3-yl}prop-2-enoic acid, 3-(2-Carboxyethenyl)-1-[(4-methylphenyl)sulphonyl]-1H-indole;(E)-3-(1-tosyl-1H-indol-3-yl)acrylicacid;(2E)-3-[1-(4-methylbenzenesulfonyl)-1H-indol-3-yl]prop-2-enoic acid
    3. CAS NO:298187-97-0
    4. Molecular Formula: C18H15NO4S
    5. Molecular Weight: 341.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 298187-97-0.mol
  • Chemical Properties

    1. Melting Point: 238 °C
    2. Boiling Point: 588.1°Cat760mmHg
    3. Flash Point: 309.5°C
    4. Appearance: /
    5. Density: 1.3g/cm3
    6. Vapor Pressure: 1.12E-14mmHg at 25°C
    7. Refractive Index: 1.63
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 4.19±0.10(Predicted)
    11. CAS DataBase Reference: 3-(1-[(4-METHYLPHENYL)SULFONYL]-1H-INDOL-3-YL)ACRYLIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-(1-[(4-METHYLPHENYL)SULFONYL]-1H-INDOL-3-YL)ACRYLIC ACID(298187-97-0)
    13. EPA Substance Registry System: 3-(1-[(4-METHYLPHENYL)SULFONYL]-1H-INDOL-3-YL)ACRYLIC ACID(298187-97-0)
  • Safety Data

    1. Hazard Codes:  Xi:Irritant;
    2. Statements: R36/37/38:Irritating to eyes, respiratory system and skin.;
    3. Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S37/39:Wear suitable g
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 298187-97-0(Hazardous Substances Data)

298187-97-0 Usage

Uses

Used in Pharmaceutical Research and Drug Discovery:
MSIA is employed as a starting material for the synthesis of bioactive molecules due to its unique structure and reactivity. It is particularly of interest for the development of novel drugs with potential therapeutic properties.
Used in Anti-inflammatory Applications:
MSIA is used as an anti-inflammatory agent, leveraging its potential to modulate inflammatory pathways and provide relief from inflammation-related conditions.
Used in Anti-cancer Applications:
In the field of oncology, MSIA is utilized as an anti-cancer agent, showing promise in the development of treatments for various types of cancer. Its anti-cancer activities are being studied for their potential to contribute to cancer therapy.
Used in Organic Synthesis:
MSIA serves as a building block in organic synthesis, allowing chemists to create complex organic molecules with unique functional groups, which can be applied across different industries and research areas.
Used in Chemical Compound Development:
MSIA is used in the development of new chemical compounds with potential applications in various fields, including but not limited to pharmaceuticals, materials science, and agrochemicals, due to its versatile chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 298187-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,8,1,8 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 298187-97:
(8*2)+(7*9)+(6*8)+(5*1)+(4*8)+(3*7)+(2*9)+(1*7)=210
210 % 10 = 0
So 298187-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H15NO4S/c1-13-6-9-15(10-7-13)24(22,23)19-12-14(8-11-18(20)21)16-4-2-3-5-17(16)19/h2-12H,1H3,(H,20,21)/b11-8+

298187-97-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-[(4-METHYLPHENYL)SULFONYL]-1H-INDOL-3-YL)ACRYLIC ACID

1.2 Other means of identification

Product number -
Other names 3-{1-[(4-methylphenyl)sulphonyl]-1H-indol-3-yl}acrylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:298187-97-0 SDS

298187-97-0Downstream Products

298187-97-0Relevant articles and documents

Highly efficient and stereoselective N-vinylation of oxiranecarboxamides and unprecedented 8-endo-epoxy-arene cyclization: Expedient and biomimetic synthesis of some clausena alkaloids

Yang, Luo,Deng, Gang,Wang, De-Xian,Huang, Zhi-Tang,Zhu, Jie-Ping,Wang, Mei-Xiang

, p. 1387 - 1390 (2007/10/03)

Figure presented Catalyzed by Cul/N,N-dimethylglycine, oxiranecarboxamides underwent a highly efficient and stereoselective N-vinylation reaction with (Z)-1-aryl-2-bromoethenes to afford the corresponding enamides. The method has been applied to a straigh

The Total Synthesis of (+)-Hapalindole Q by an Organomediated Diels-Alder Reaction

Kinsman, Aaron C.,Kerr, Michael A.

, p. 14120 - 14125 (2007/10/03)

The total synthesis of (+)-hapalindole Q has been achieved. The key step is a Diels-Alder reaction mediated by MacMillan's organocatalyst to provide the critical intermediate with high enantiose-lectivity (93% ee). This step establishes the proper arrange

Synthesis and serotonin receptor affinities of a series of trans-2- (indol-3-yl)cyclopropylamine derivatives

Vangveravong, Suwanna,Kanthasamy, Arthi,Lucaites, Virginia L.,Nelson, David L.,Nichols, David E.

, p. 4995 - 5001 (2007/10/03)

A series of four racemic ring-substituted trans-2-(indol-3- yl)cyclopropylamine derivatives was synthesized and tested for affinity at the 5-HT(1A) receptor, by competition with [3H]-8-OH-DPAT in rat hippocampal homogenates, and for affinity at

Stereoselective Synthesis of trans-2-(Indol-3-yl)cyclopropylamines: Rigid Tryptamine Analogues

Vangveravong, Suwanna,Nichols, David E.

, p. 3409 - 3413 (2007/10/02)

A procedure for the preparation of trans-2-(indol-3-yl)cyclopropylamines is reported.The key step in the sequence is a stereoselective palladium-catalyzed cyclopropanation of the indole-3-acryloyl derivative of Oppolzer's chiral sultam (bornanesulta

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