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CAS

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261712-19-0

toluene-4-thiosulfonic acid S-(4,5-bis-tert-butoxycarbonylamino-2-tert-butyl-phenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 261712-19-0 Structure

  • Basic information

    1. Product Name: toluene-4-thiosulfonic acid S-(4,5-bis-tert-butoxycarbonylamino-2-tert-butyl-phenyl) ester
    2. Synonyms: toluene-4-thiosulfonic acid S-(4,5-bis-tert-butoxycarbonylamino-2-tert-butyl-phenyl) ester
    3. CAS NO:261712-19-0
    4. Molecular Formula:
    5. Molecular Weight: 550.741
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 261712-19-0.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: toluene-4-thiosulfonic acid S-(4,5-bis-tert-butoxycarbonylamino-2-tert-butyl-phenyl) ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: toluene-4-thiosulfonic acid S-(4,5-bis-tert-butoxycarbonylamino-2-tert-butyl-phenyl) ester(261712-19-0)
    11. EPA Substance Registry System: toluene-4-thiosulfonic acid S-(4,5-bis-tert-butoxycarbonylamino-2-tert-butyl-phenyl) ester(261712-19-0)

  • 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: 261712-19-0(Hazardous Substances Data)

261712-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261712-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,7,1 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 261712-19:
(8*2)+(7*6)+(6*1)+(5*7)+(4*1)+(3*2)+(2*1)+(1*9)=120
120 % 10 = 0
So 261712-19-0 is a valid CAS Registry Number.

261712-19-0Relevant articles and documents

HIV protease inhibitors

-

, (2008/06/13)

The present invention relates to novel dihydropyrones with tethered heterocycles having improved pharmacologic properties which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The dihydropyrones are useful in the development of therapies for the treatment of viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of the dihydropyrones and intermediates useful in the preparation of the final compounds.

Synthesis of heterocyclic thiosulfonates

Vara Prasad

, p. 1069 - 1072 (2007/10/03)

A simple synthesis of heterocyclic thiosulfonates containing indole, indoline, benzoimidazole, and quinoxaline rings is described. The synthesis of these thiosulfonates involves the preparation of the appropriately substituted thiols followed by sulfonyla

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