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CAS

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845626-33-7

C17H24N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 845626-33-7 Structure

  • Basic information

    1. Product Name: C17H24N2O2
    2. Synonyms: C17H24N2O2
    3. CAS NO:845626-33-7
    4. Molecular Formula:
    5. Molecular Weight: 288.39
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 845626-33-7.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: C17H24N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H24N2O2(845626-33-7)
    11. EPA Substance Registry System: C17H24N2O2(845626-33-7)

  • 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: 845626-33-7(Hazardous Substances Data)

845626-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 845626-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,6,2 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 845626-33:
(8*8)+(7*4)+(6*5)+(5*6)+(4*2)+(3*6)+(2*3)+(1*3)=187
187 % 10 = 7
So 845626-33-7 is a valid CAS Registry Number.

845626-33-7Downstream Products

845626-33-7Relevant articles and documents

Rifamycin analogs and uses thereof

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Page/Page column 20, (2008/06/13)

The present invention features rifamycin analogs and methods of using these compounds to treat a variety of microbial infections.

Rifamycin analogs and uses thereof

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Page/Page column 38-39, (2008/06/13)

The present invention features rifamycin analogs that can be used as therapeutics for treating or preventing a variety of microbial infections. In one form, the analogs are acetylated at the 25-position, as is rifamycin. In another form, the analogs are deacetylated at the 25-position. In yet other forms, benzoxazinorifamycin, benzthiazinorifamycin, and benzdiazinorifamycin analogs are derivatized at various positions of the benzene ring, including 3′-hydroxy analogs, 4′- and/or 6′ halo and/or alkoxy analogs, and various 5′ substituents that incorporate a cyclic amine moiety.

Rifamycin analogs and uses thereof

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Page/Page column 34, (2008/06/13)

The present invention features rifamycin analogs that can be used as therapeutics for treating or preventing a variety of microbial infections. In one form, the analogs are acetylated at the 25-position, as is rifamycin. In another form, the analogs are deacetylated at the 25-position. In yet other forms, benzoxazinorifamycin, benzthiazinorifamycin, and benzdiazinorifamycin analogs are derivatized at various positions of the benzene ring, including 3′-hydroxy analogs, 4′-and/or 6′ halo and/or alkoxy analogs, and various 5′ substituents that incorporate a cyclic amine moiety.

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