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99532-51-1

1-(Phenylsulfonyl)-1H-indole-3-carbonyl chloride is a chemical compound that features a phenylsulfonyl group and a carbonyl chloride group attached to an indole ring. It is widely recognized for its reactivity with a broad spectrum of nucleophiles, which makes it a versatile reagent in organic synthesis for introducing carbonyl chloride functionality into a variety of organic molecules.

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  • 99532-51-1 Structure

  • Basic information

    1. Product Name: 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBONYL CHLORIDE
    2. Synonyms: 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBONYL CHLORIDE;1-PHENYLSULPHONYLINDOLE-3-CARBONYL CHLORIDE;1-(Phenylsulphonyl)-1H-indole-3-carbonyl chloride;1-PHENYLSULFONYLINDOLE-3-CARBONYL CHLORIDE
    3. CAS NO:99532-51-1
    4. Molecular Formula: C15H10ClNO3S
    5. Molecular Weight: 319.76
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 99532-51-1.mol

  • Chemical Properties

    1. Melting Point: 144 °C
    2. Boiling Point: 515.6°C at 760 mmHg
    3. Flash Point: 265.6°C
    4. Appearance: /
    5. Density: 1.41g/cm3
    6. Vapor Pressure: 9.67E-11mmHg at 25°C
    7. Refractive Index: 1.656
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBONYL CHLORIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBONYL CHLORIDE(99532-51-1)
    12. EPA Substance Registry System: 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBONYL CHLORIDE(99532-51-1)

  • Safety Data

    1. Hazard Codes: C,Xi
    2. Statements: 36
    3. Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S36/37/39:Wear suitabl
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 99532-51-1(Hazardous Substances Data)

99532-51-1 Usage

Uses

Used in Organic Synthesis:
1-(Phenylsulfonyl)-1H-indole-3-carbonyl chloride is used as a reagent for introducing carbonyl chloride functionality into organic molecules, which is crucial for the synthesis of a diverse range of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(Phenylsulfonyl)-1H-indole-3-carbonyl chloride is utilized for the synthesis of potential drug candidates. Its unique structure and reactivity contribute to the development of new compounds with therapeutic potential.
Used in Material Science:
1-(Phenylsulfonyl)-1H-indole-3-carbonyl chloride is also employed in the development of new materials and compounds for various applications across different industries, thanks to its ability to react with multiple nucleophiles and form a wide array of products.

Check Digit Verification of cas no

The CAS Registry Mumber 99532-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,3 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99532-51:
(7*9)+(6*9)+(5*5)+(4*3)+(3*2)+(2*5)+(1*1)=171
171 % 10 = 1
So 99532-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClNO3S/c16-15(18)13-10-17(14-9-5-4-8-12(13)14)21(19,20)11-6-2-1-3-7-11/h1-10H

99532-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfonyl)indole-3-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 3-(chlorocarbonyl)-1-(phenylsulfonyl)-1H-indole

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:99532-51-1 SDS

99532-51-1Relevant articles and documents

Synthesis and biological evaluation of bengacarboline derivatives

Pouilhes, Annie,Kouklovsky, Cyrille,Langlois, Yves,Baltaze, Jean-Pierre,Vispe, Stephane,Annereau, Jean-Philippe,Barret, Jean-Marc,Kruczynski, Anna,Bailly, Christian

, p. 1212 - 1216 (2008/12/21)

Novel derivatives of the marine alkaloid bengacarboline have been synthesized. The seco derivatives 11 and 12 were evaluated for topoisomerase inhibition, DNA damages, cytotoxicity and cell cycle perturbation. The two synthetic analogs are more potent cyt

First synthesis of marine alkaloid (±)-bengacarboline

Pouilhès, Annie,Langlois, Yves,Chiaroni, Angèle

, p. 1488 - 1490 (2007/10/03)

Bengacarboline 1, a marine alkaloid, potent inhibitor of topoisomerase II, has been synthesized in nine steps from indol-3-carboxylic acid and tryptamine.

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