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299434-06-3

C30H38O9 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 299434-06-3 Structure

  • Basic information

    1. Product Name: C30H38O9
    2. Synonyms:
    3. CAS NO:299434-06-3
    4. Molecular Formula:
    5. Molecular Weight: 542.626
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 299434-06-3.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: C30H38O9(CAS DataBase Reference)
    10. NIST Chemistry Reference: C30H38O9(299434-06-3)
    11. EPA Substance Registry System: C30H38O9(299434-06-3)

  • 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: 299434-06-3(Hazardous Substances Data)

299434-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 299434-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,4,3 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 299434-06:
(8*2)+(7*9)+(6*9)+(5*4)+(4*3)+(3*4)+(2*0)+(1*6)=183
183 % 10 = 3
So 299434-06-3 is a valid CAS Registry Number.

299434-06-3Downstream Products

299434-06-3Relevant articles and documents

Synthesis of New Diols Derived from Dianhydrohexitols Ethers under Microwave-Assisted Phase Transfer Catalysis

Chatti, Saber,Bortolussi, Michel,Loupy, André

, p. 5877 - 5883 (2000)

Alkylation of mono-benzylated isosorbide and isomannide was performed under microwave assisted phase transfer catalysis (PTC). A small amount of solvent was necessary to provide good yields (90-96%) within 15 min. In order to minimize the competitive elimination, halide leaving group was changed to tosylate as competitive S(N)2-E2 processes were involved. After removal of benzyl moiety by hydrogenation, a series of new diols from dianhydrohexitols were thus prepared. (C) 2000 Elsevier Science Ltd.

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