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1422364-39-3

C45H60N2O12S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1422364-39-3 Structure

  • Basic information

    1. Product Name: C45H60N2O12S
    2. Synonyms: C45H60N2O12S
    3. CAS NO:1422364-39-3
    4. Molecular Formula:
    5. Molecular Weight: 853.044
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1422364-39-3.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: C45H60N2O12S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C45H60N2O12S(1422364-39-3)
    11. EPA Substance Registry System: C45H60N2O12S(1422364-39-3)

  • 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: 1422364-39-3(Hazardous Substances Data)

1422364-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1422364-39-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,3,6 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1422364-39:
(9*1)+(8*4)+(7*2)+(6*2)+(5*3)+(4*6)+(3*4)+(2*3)+(1*9)=133
133 % 10 = 3
So 1422364-39-3 is a valid CAS Registry Number.

1422364-39-3Downstream Products

1422364-39-3Relevant articles and documents

Synthesis, antibacterial activity and docking of 14-membered 9-O-(3-arylalkyl) oxime 11,12-cyclic carbonate ketolides

Liang, Jian-Hua,An, Kun,Lv, Wei,Cushman, Mark,Wang, He,Xu, Ying-Chun

, p. 54 - 63 (2013)

A series of 9-O-(3-aryl-2-propargyl)oxime ketolides 8 was synthesized and evaluated for in vitro antibacterial activity. Among 8, 8b-8d, and 8h-8l displayed dramatically improved potency against inducibly MLS B-resistant and efflux-resistant pathogens as compared to clarithromycin and azithromycin. Especially, 8i (Ar4-isoquinolyl) possessed an MIC of 0.064 μg/mL against constitutively MLSB-resistant Streptococcus pneumoniae, and MICs of 0.032-0.064 μg/mL against methicillin-resistant Staphylococcus aureus and methicillin-resistant Staphylococcus hominis. The analog 10 with a propyl linker was less effective than both the corresponding 8 and 9 containing propynyl and propenyl linkers. A docking study was performed to gain insight into the binding mode of series 8 and 9 and to rationalize the disparity found in the SAR of 8 and 9.

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