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129667-06-7

2-cyclohexanoyl-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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  • 129667-06-7 Structure

  • Basic information

    1. Product Name: 2-cyclohexanoyl-1-tosylpyrrole
    2. Synonyms: 2-cyclohexanoyl-1-tosylpyrrole
    3. CAS NO:129667-06-7
    4. Molecular Formula:
    5. Molecular Weight: 331.436
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129667-06-7.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: 2-cyclohexanoyl-1-tosylpyrrole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-cyclohexanoyl-1-tosylpyrrole(129667-06-7)
    11. EPA Substance Registry System: 2-cyclohexanoyl-1-tosylpyrrole(129667-06-7)

  • 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: 129667-06-7(Hazardous Substances Data)

129667-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129667-06-7 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 129667-06:
(8*1)+(7*2)+(6*9)+(5*6)+(4*6)+(3*7)+(2*0)+(1*6)=157
157 % 10 = 7
So 129667-06-7 is a valid CAS Registry Number.

129667-06-7Relevant 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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