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CAS

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215164-33-3

4-[2,6-Bis-(toluene-4-sulfonyloxymethyl)-pyridin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 215164-33-3 Structure

  • Basic information

    1. Product Name: 4-[2,6-Bis-(toluene-4-sulfonyloxymethyl)-pyridin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester
    2. Synonyms:
    3. CAS NO:215164-33-3
    4. Molecular Formula:
    5. Molecular Weight: 631.771
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 215164-33-3.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: 4-[2,6-Bis-(toluene-4-sulfonyloxymethyl)-pyridin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[2,6-Bis-(toluene-4-sulfonyloxymethyl)-pyridin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester(215164-33-3)
    11. EPA Substance Registry System: 4-[2,6-Bis-(toluene-4-sulfonyloxymethyl)-pyridin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester(215164-33-3)

  • 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: 215164-33-3(Hazardous Substances Data)

215164-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215164-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,1,6 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 215164-33:
(8*2)+(7*1)+(6*5)+(5*1)+(4*6)+(3*4)+(2*3)+(1*3)=103
103 % 10 = 3
So 215164-33-3 is a valid CAS Registry Number.

215164-33-3Relevant articles and documents

New piperazinyl polyazacyclophane scaffolds, libraries and biological activities

An, Haoyun,Haly, Becky D.,Cook, P. Dan

, p. 2345 - 2350 (1998)

Four novel unsymmetric piperazinyl polyazacyclophane scaffolds 1-4 were synthesized in high yields by an efficient cyclization strategy. Twenty-six libraries 12-37 (total 16000 compounds) were generated by a solution-phase combinatorial approach from 1-4 and thirty-eight functional groups. Potent antibacterial and HIV-1 tat/TAR protein-RNA disrupting activities were discovered.

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