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113352-91-3

C33H36N2O4S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113352-91-3 Structure

  • Basic information

    1. Product Name: C33H36N2O4S
    2. Synonyms:
    3. CAS NO:113352-91-3
    4. Molecular Formula:
    5. Molecular Weight: 556.726
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 113352-91-3.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: C33H36N2O4S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C33H36N2O4S(113352-91-3)
    11. EPA Substance Registry System: C33H36N2O4S(113352-91-3)

  • 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: 113352-91-3(Hazardous Substances Data)

113352-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113352-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 113352-91:
(8*1)+(7*1)+(6*3)+(5*3)+(4*5)+(3*2)+(2*9)+(1*1)=93
93 % 10 = 3
So 113352-91-3 is a valid CAS Registry Number.

113352-91-3Relevant articles and documents

Methods for Indole Alkaloid Synthesis: A Study of the Compatibility of the Indole-2,3-Quinodimethane Strategy for the Synthesis of 16-Methoxy-Substituted Aspidosperma-Type Alkaloids. Synthesis of (+)- and (-)-16-Methoxytabersonine

Cardwell, Kevin,Hewitt, Brian,Ladlow, Mark,Magnus, Philip

, p. 2242 - 2248 (2007/10/02)

4-Methoxy-2-nitroaniline (5) is converted into 1-carbomethoxy-6-methoxy-3-formyl-2-methylindole (10) in an overall yield of 28percent through five steps.The derived imine from 10 and 2-(phenylthio)ethylamine on treatment with acid chloride (+/-)-12 gave h

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