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1037075-04-9

[B((S)-VAPOL(2-))(phenoxy)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1037075-04-9 Structure

  • Basic information

    1. Product Name: [B((S)-VAPOL(2-))(phenoxy)]
    2. Synonyms:
    3. CAS NO:1037075-04-9
    4. Molecular Formula:
    5. Molecular Weight: 640.545
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1037075-04-9.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: [B((S)-VAPOL(2-))(phenoxy)](CAS DataBase Reference)
    10. NIST Chemistry Reference: [B((S)-VAPOL(2-))(phenoxy)](1037075-04-9)
    11. EPA Substance Registry System: [B((S)-VAPOL(2-))(phenoxy)](1037075-04-9)

  • 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: 1037075-04-9(Hazardous Substances Data)

1037075-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1037075-04-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,0,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1037075-04:
(9*1)+(8*0)+(7*3)+(6*7)+(5*0)+(4*7)+(3*5)+(2*0)+(1*4)=119
119 % 10 = 9
So 1037075-04-9 is a valid CAS Registry Number.

1037075-04-9Downstream Products

1037075-04-9Relevant articles and documents

Substrate-induced covalent assembly of a chemzyme and crystallographic characterization of a chemzyme-substrate complex

Hu, Gang,Gupta, Anil K.,Huang, Rui H.,Mukherjee, Munmun,Wulff, William D.

, p. 14669 - 14675 (2010/12/25)

A substrate induced covalent assembly of a highly organized chemzyme known to be effective in both catalytic asymmetric aziridination and aza Diels-Alder reactions is described and the information gained from which led to an efficient one-pot aziridination protocol. The crystal structures of two chemzyme-iminium complexes were elucidated by X-ray diffraction analysis that provides critical insights into the binding of the substrates with the chemzyme.

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