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135039-99-5

N,N-Diethyl-2-methyl-1-phenylsulfonylindole-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135039-99-5 Structure

  • Basic information

    1. Product Name: N,N-Diethyl-2-methyl-1-phenylsulfonylindole-3-carboxamide
    2. Synonyms:
    3. CAS NO:135039-99-5
    4. Molecular Formula:
    5. Molecular Weight: 370.472
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135039-99-5.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: N,N-Diethyl-2-methyl-1-phenylsulfonylindole-3-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-Diethyl-2-methyl-1-phenylsulfonylindole-3-carboxamide(135039-99-5)
    11. EPA Substance Registry System: N,N-Diethyl-2-methyl-1-phenylsulfonylindole-3-carboxamide(135039-99-5)

  • 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: 135039-99-5(Hazardous Substances Data)

135039-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135039-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,3 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135039-99:
(8*1)+(7*3)+(6*5)+(5*0)+(4*3)+(3*9)+(2*9)+(1*9)=125
125 % 10 = 5
So 135039-99-5 is a valid CAS Registry Number.

135039-99-5Relevant articles and documents

Preparation of 2,3-Disubstituted Indoles from Indole-3-carboxylic Acids and Amides by α-Deprotonation

Buttery, Cheryl D.,Jones, Richard G.,Knight, David W.

, p. 1425 - 1432 (2007/10/02)

Direct deprotonations have been used to obtain the 2(α)-lithiated indole-3-carboxylate dianions 8 and 14, together with the related 2(α)-lithiated indole-3-carboxamide monoanions 18 and 20b from the parent compounds.These four intermediates are useful for

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