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1427037-97-5

C24H34O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1427037-97-5 Structure

  • Basic information

    1. Product Name: C24H34O3
    2. Synonyms:
    3. CAS NO:1427037-97-5
    4. Molecular Formula:
    5. Molecular Weight: 370.532
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427037-97-5.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: C24H34O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H34O3(1427037-97-5)
    11. EPA Substance Registry System: C24H34O3(1427037-97-5)

  • 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: 1427037-97-5(Hazardous Substances Data)

1427037-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427037-97-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,0,3 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1427037-97:
(9*1)+(8*4)+(7*2)+(6*7)+(5*0)+(4*3)+(3*7)+(2*9)+(1*7)=155
155 % 10 = 5
So 1427037-97-5 is a valid CAS Registry Number.

1427037-97-5Downstream Products

1427037-97-5Relevant articles and documents

Bioactive indole alkaloids and phenyl ether derivatives from a marine-derived Aspergillus sp. fungus

Chen, Min,Shao, Chang-Lun,Fu, Xiu-Mei,Xu, Ru-Fang,Zheng, Juan-Juan,Zhao, Dong-Lin,She, Zhi-Gang,Wang, Chang-Yun

, p. 547 - 553 (2013)

Two new prenylated indole alkaloids, 17-epi-notoamides Q and M (1 and 2), and two new phenyl ether derivatives, cordyols D and E (9 and 13), together with 10 known compounds (3-8, 10-12, 14) were isolated from a marine-derived Aspergillus sp. fungus. Among them, 1/5 and 2/4 were pairs of epimers. The planar structures and absolute configurations of the new compounds were determined by extensive NMR spectroscopic data as well as CD spectra. The absolute configuration of 3 was confirmed by single-crystal X-ray diffraction analysis for the first time. All isolated metabolites (1-14) and eight synthetic phenyl ether derivatives (12a, 14a-14g) were evaluated for their antibacterial activities in vitro. The polybromide phenyl ether 14g showed pronounced antibacterial activity against Staphylococcus epidermidis with an MIC value of 0.556 μM, stronger than that of the positive control ciprofloxacin (MIC = 3.13 μM).

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