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5-ethyl-1-(phenylsulfonyl)indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118757-09-8 Structure
  • Basic information

    1. Product Name: 5-ethyl-1-(phenylsulfonyl)indole
    2. Synonyms: 5-ethyl-1-(phenylsulfonyl)indole
    3. CAS NO:118757-09-8
    4. Molecular Formula:
    5. Molecular Weight: 285.367
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118757-09-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-ethyl-1-(phenylsulfonyl)indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-ethyl-1-(phenylsulfonyl)indole(118757-09-8)
    11. EPA Substance Registry System: 5-ethyl-1-(phenylsulfonyl)indole(118757-09-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 118757-09-8(Hazardous Substances Data)

118757-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118757-09-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,5 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118757-09:
(8*1)+(7*1)+(6*8)+(5*7)+(4*5)+(3*7)+(2*0)+(1*9)=148
148 % 10 = 8
So 118757-09-8 is a valid CAS Registry Number.

118757-09-8Downstream Products

118757-09-8Relevant articles and documents

Synthesis of Alkyl-Substituted N-Protected Indoles via Acylation and Reductive Deoxygenation

Ketcha, Daniel M.,Lieurance, Brett A.,Homan, Dominic F. J.,Gribble, Gordin W.

, p. 4350 - 4356 (2007/10/02)

The synthesis of 2-, 3-, and 5-alkyl-1-(phenylsulfonyl)indoles involving Friedel-Crafts acylation followed by reductive deoxygenation is described.The application of this acylation-deoxygenation sequence to 3-acyl-1-(phenylsulfonyl)indoles bearing potenti

THE MANGANESE(III) ACETATE OXIDATION OF N-PROTECTED INDOLINES

Ketcha, Daniel M.

, p. 2151 - 2154 (2007/10/02)

A variety of N-protected indolines can be oxidized to the corresponding indoles using manganese(III) acetate in glacial acetic acid.

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