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3-(3-ethoxycarbonylpropanoyl)-1-tosylpyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129667-09-0 Structure
  • Basic information

    1. Product Name: 3-(3-ethoxycarbonylpropanoyl)-1-tosylpyrrole
    2. Synonyms:
    3. CAS NO:129667-09-0
    4. Molecular Formula:
    5. Molecular Weight: 349.408
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129667-09-0.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: 3-(3-ethoxycarbonylpropanoyl)-1-tosylpyrrole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3-ethoxycarbonylpropanoyl)-1-tosylpyrrole(129667-09-0)
    11. EPA Substance Registry System: 3-(3-ethoxycarbonylpropanoyl)-1-tosylpyrrole(129667-09-0)
  • 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: 129667-09-0(Hazardous Substances Data)

129667-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129667-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129667-09:
(8*1)+(7*2)+(6*9)+(5*6)+(4*6)+(3*7)+(2*0)+(1*9)=160
160 % 10 = 0
So 129667-09-0 is a valid CAS Registry Number.

129667-09-0Downstream Products

129667-09-0Relevant articles and documents

PREPARATION OF ALKYL-SUBSTITUTED INDOLES IN THE BENZENE PORTION. Part 3

Muratake, Hideaki,Natsume, Mitsutaka

, p. 683 - 690 (2007/10/02)

Three-step synthesis of 7- and 4-alkyl-1-tosylindoles (9 and 10) was accomplished by combination of the Friedel-Crafts acylation of 4, and the treatment of 7 and 8 with H2SO4 in 2-propanol as illustrated in Chart 2.Further a novel synthetic method of 16 was devised from 14 by way of 15.

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