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CAS

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433713-62-3

[4-(1R,4R,5R,8R)-8-benzyloxy-2,6-dioxabicyclo[3.3.0]octane]-(2-oxo-2-phenyl)-ethanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 433713-62-3 Structure

  • Basic information

    1. Product Name: [4-(1R,4R,5R,8R)-8-benzyloxy-2,6-dioxabicyclo[3.3.0]octane]-(2-oxo-2-phenyl)-ethanoate
    2. Synonyms: [4-(1R,4R,5R,8R)-8-benzyloxy-2,6-dioxabicyclo[3.3.0]octane]-(2-oxo-2-phenyl)-ethanoate
    3. CAS NO:433713-62-3
    4. Molecular Formula:
    5. Molecular Weight: 368.386
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 433713-62-3.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: [4-(1R,4R,5R,8R)-8-benzyloxy-2,6-dioxabicyclo[3.3.0]octane]-(2-oxo-2-phenyl)-ethanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: [4-(1R,4R,5R,8R)-8-benzyloxy-2,6-dioxabicyclo[3.3.0]octane]-(2-oxo-2-phenyl)-ethanoate(433713-62-3)
    11. EPA Substance Registry System: [4-(1R,4R,5R,8R)-8-benzyloxy-2,6-dioxabicyclo[3.3.0]octane]-(2-oxo-2-phenyl)-ethanoate(433713-62-3)

  • 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: 433713-62-3(Hazardous Substances Data)

433713-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 433713-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,7,1 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 433713-62:
(8*4)+(7*3)+(6*3)+(5*7)+(4*1)+(3*3)+(2*6)+(1*2)=133
133 % 10 = 3
So 433713-62-3 is a valid CAS Registry Number.

433713-62-3Downstream Products

433713-62-3Relevant articles and documents

Isomannide and isosorbide as new chiral auxiliaries for the stereoselective synthesis of tertiary α-hydroxy acids

Loupy, André,Monteux, Daphné A

, p. 1541 - 1549 (2002)

Isomannide and isosorbide are selectively protected to provide new chiral auxiliaries suitable for the preparation of enantiopure tertiary α-hydroxy acids. Diastereoselective additions of organozinc reagents on the derived phenylglyoxylates afford the desired α-hydroxy acids with 60-99% ee after saponification. Both absolute configurations of the α-hydroxy acids can be accessed, by adapted choice of either the starting diol or the protecting group.

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