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146253-75-0

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  • 146253-75-0 Structure

  • Basic information

    1. Product Name: 13-(benzylthio)-5-hydroxy-6-α-deoxytetracycline
    2. Synonyms: 13-(benzylthio)-5-hydroxy-6-α-deoxytetracycline
    3. CAS NO:146253-75-0
    4. Molecular Formula:
    5. Molecular Weight: 566.632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146253-75-0.mol
    9. Article Data: 1

  • 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: 13-(benzylthio)-5-hydroxy-6-α-deoxytetracycline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 13-(benzylthio)-5-hydroxy-6-α-deoxytetracycline(146253-75-0)
    11. EPA Substance Registry System: 13-(benzylthio)-5-hydroxy-6-α-deoxytetracycline(146253-75-0)

  • 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: 146253-75-0(Hazardous Substances Data)

146253-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146253-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,2,5 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 146253-75:
(8*1)+(7*4)+(6*6)+(5*2)+(4*5)+(3*3)+(2*7)+(1*5)=130
130 % 10 = 0
So 146253-75-0 is a valid CAS Registry Number.

146253-75-0Downstream Products

146253-75-0Relevant articles and documents

Inhibition of the Tetracycline Efflux Antiport Protein by 13-Thio-Substituted 5-Hydroxy-6-deoxytetracyclines

Nelson, Mark L.,Park, Britt H.,Andrews, Janey S.,Georgian, Vlasios A.,Thomas, Richard C.,Levy, Stuart B.

, p. 370 - 377 (1993)

A series of 13-(alkylthio) and 13-(arylthio) derivatives of 5-hydroxy-6-deoxytetracycline (tetracycline, Tc) were synthesized and compared to the clinically used antibiotics tetracycline, methacycline, and minocycline for their ability to inhibit tetracyc

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