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CAS

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1458033-21-0

(R)-2-((1R,2R)-4-(benzyloxy)-1-(methoxymethoxy)-2-methylbutyl)oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1458033-21-0 Structure

  • Basic information

    1. Product Name: (R)-2-((1R,2R)-4-(benzyloxy)-1-(methoxymethoxy)-2-methylbutyl)oxirane
    2. Synonyms: (R)-2-((1R,2R)-4-(benzyloxy)-1-(methoxymethoxy)-2-methylbutyl)oxirane
    3. CAS NO:1458033-21-0
    4. Molecular Formula:
    5. Molecular Weight: 280.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1458033-21-0.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: (R)-2-((1R,2R)-4-(benzyloxy)-1-(methoxymethoxy)-2-methylbutyl)oxirane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-((1R,2R)-4-(benzyloxy)-1-(methoxymethoxy)-2-methylbutyl)oxirane(1458033-21-0)
    11. EPA Substance Registry System: (R)-2-((1R,2R)-4-(benzyloxy)-1-(methoxymethoxy)-2-methylbutyl)oxirane(1458033-21-0)

  • 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: 1458033-21-0(Hazardous Substances Data)

1458033-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1458033-21-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,8,0,3 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1458033-21:
(9*1)+(8*4)+(7*5)+(6*8)+(5*0)+(4*3)+(3*3)+(2*2)+(1*1)=150
150 % 10 = 0
So 1458033-21-0 is a valid CAS Registry Number.

1458033-21-0Relevant articles and documents

Total synthesis of attenols A and B

Reddy, B.V. Subba,Reddy, B. Phaneendra,Swapnil,Yadav

, p. 5781 - 5784 (2013/10/01)

A concise approach for the total synthesis of attenols A and B is described involving MacMillan's α-aminooxylation, Evan's asymmetric alkylation, Brown's allylation, and spiro-ketalization as key steps. This approach has successfully demonstrated the α-aminooxylation protocol for the construction of the anti-1,3-diol unit.

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