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CAS

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791101-23-0

C16H22O5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 791101-23-0 Structure

  • Basic information

    1. Product Name: C16H22O5
    2. Synonyms: C16H22O5
    3. CAS NO:791101-23-0
    4. Molecular Formula:
    5. Molecular Weight: 294.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 791101-23-0.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: C16H22O5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H22O5(791101-23-0)
    11. EPA Substance Registry System: C16H22O5(791101-23-0)

  • 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: 791101-23-0(Hazardous Substances Data)

791101-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 791101-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,1,0 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 791101-23:
(8*7)+(7*9)+(6*1)+(5*1)+(4*0)+(3*1)+(2*2)+(1*3)=140
140 % 10 = 0
So 791101-23-0 is a valid CAS Registry Number.

791101-23-0Downstream Products

791101-23-0Relevant articles and documents

Total synthesis of catenioblin B

Srinivas, Theegala,Hügel, Helmut M.,Radha Krishna, Palakodety

, p. 5952 - 5954 (2014)

Herein we report the first total synthesis of catenioblin B (1) via a titanium(IV) mediated regioselective epoxide ring-opening, Grignard reaction, Luche's reduction and TEMPO/BAIB mediated intramolecular cyclization as the key steps.

Discovery of a potent, metabolically stabilized resorcylic lactone as an anti-inflammatory lead

Du,Matsushima,Spyvee,Goto,Shirota,Gusovsky,Chiba,Kotake,Yoneda,Eguchi,DiPietro,Harmange,Gilbert,Li,Davis,Jiang,Zhang,Pelletier,Wong,Sakurai,Yang,Ito-Igarashi,Kimura,Kuboi,Mizui,Tanaka,Ikemori-Kawada,Kawakami,Inoue,Kawai,Kishi,Wang

supporting information; scheme or table, p. 6196 - 6199 (2010/06/19)

With bioactivity-guided phenotype screenings, a potent anti-inflammatory compound f152A1 has been isolated, characterized and identified as the known natural product LL-Z1640-2. Metabolic instability precluded its use for the study on animal disease model

MACROCYCLIC COMPOUNDS USEFUL AS PHARMACEUTICALS

-

Page/Page column 97, (2010/02/07)

The present invention provides compounds having formula (I), and additionally provides methods for the synthesis thereof and methods for the use thereof in the treatment of various disorders including inflammatory or autoimmune disorders, and disorders involving malignancy or increased angiogenesis, wherein R1 -R11, t, X, Y, Z, and n are as defined herein.

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