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CAS

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552298-25-6

((((2S,4R)-5-iodo-2,4-dimethylpentyl)oxy)methyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 552298-25-6 Structure

  • Basic information

    1. Product Name: ((((2S,4R)-5-iodo-2,4-dimethylpentyl)oxy)methyl)benzene
    2. Synonyms: ((((2S,4R)-5-iodo-2,4-dimethylpentyl)oxy)methyl)benzene
    3. CAS NO:552298-25-6
    4. Molecular Formula:
    5. Molecular Weight: 332.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 552298-25-6.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: ((((2S,4R)-5-iodo-2,4-dimethylpentyl)oxy)methyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((((2S,4R)-5-iodo-2,4-dimethylpentyl)oxy)methyl)benzene(552298-25-6)
    11. EPA Substance Registry System: ((((2S,4R)-5-iodo-2,4-dimethylpentyl)oxy)methyl)benzene(552298-25-6)

  • 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: 552298-25-6(Hazardous Substances Data)

552298-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 552298-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,2,2,9 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 552298-25:
(8*5)+(7*5)+(6*2)+(5*2)+(4*9)+(3*8)+(2*2)+(1*5)=166
166 % 10 = 6
So 552298-25-6 is a valid CAS Registry Number.

552298-25-6Relevant articles and documents

Synthetic studies on borrelidin: enantioselective synthesis of the C1-C12 fragment.

Vong, Binh G,Abraham, Sunny,Xiang, Alan X,Theodorakis, Emmanuel A

, p. 1617 - 1620 (2003)

[structure: see text] An efficient, enantioselective synthesis of the C1-C12 fragment 2 of borrelidin is presented. Construction of the "skipped" polymethylene chain of 2 was accomplished by iteration of Myers' alkylation, while formation of the C3 stereocenter was achieved by Roush's asymmetric allylboration methodology.

Diverted total synthesis of the baulamycins and analogues reveals an alternate mechanism of action

Steele, Andrew D.,Ernouf, Guillaume,Lee, Young Eun,Wuest, William M.

supporting information, p. 1126 - 1129 (2018/02/23)

The baulamycins were identified as in vitro siderophore biosynthesis inhibitors. Diverted total synthesis was used to construct the natural products and eight strategic analogues, three of which had improved inhibitory activity. Biological testing then revealed that membrane damage is the predominant mode of action in Staphylococcus aureus cells.

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