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3H-Indole, 3-methyl-3-(methylthio)-2-(2-phenylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97182-93-9 Structure
  • Basic information

    1. Product Name: 3H-Indole, 3-methyl-3-(methylthio)-2-(2-phenylethenyl)-
    2. Synonyms:
    3. CAS NO:97182-93-9
    4. Molecular Formula: C18H17NS
    5. Molecular Weight: 279.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97182-93-9.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: 3H-Indole, 3-methyl-3-(methylthio)-2-(2-phenylethenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3H-Indole, 3-methyl-3-(methylthio)-2-(2-phenylethenyl)-(97182-93-9)
    11. EPA Substance Registry System: 3H-Indole, 3-methyl-3-(methylthio)-2-(2-phenylethenyl)-(97182-93-9)
  • 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: 97182-93-9(Hazardous Substances Data)

97182-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97182-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,8 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97182-93:
(7*9)+(6*7)+(5*1)+(4*8)+(3*2)+(2*9)+(1*3)=169
169 % 10 = 9
So 97182-93-9 is a valid CAS Registry Number.

97182-93-9Downstream Products

97182-93-9Relevant articles and documents

C-2-SIDE CHAIN MODIFICATION OF 2-METHYL-3-ALKYLINDOLES VIA 3-METHYLTHIOINDOLENINES: A NEW APPROACH TO PYRROLOINDOLES

Vice, Susan F.,Friesen, Richard W.,Dmitrienko, Gary I.

, p. 165 - 168 (1985)

A strategy for side chain alkylation of 2-methyl-3-alkylindoles, involving deprotonation of 3-methylthioindolenines, derived from 2-methyl-3-alkylindoles by reaction with methane sulfenyl chloride, reaction with carbon electrophiles and reduction, is outl

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