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CAS

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461044-94-0

Acetic acid (1S,2S)-2-benzyloxy-1-bromomethyl-2-(diethoxy-phosphoryl)-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 461044-94-0 Structure

  • Basic information

    1. Product Name: Acetic acid (1S,2S)-2-benzyloxy-1-bromomethyl-2-(diethoxy-phosphoryl)-ethyl ester
    2. Synonyms:
    3. CAS NO:461044-94-0
    4. Molecular Formula:
    5. Molecular Weight: 423.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 461044-94-0.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: Acetic acid (1S,2S)-2-benzyloxy-1-bromomethyl-2-(diethoxy-phosphoryl)-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid (1S,2S)-2-benzyloxy-1-bromomethyl-2-(diethoxy-phosphoryl)-ethyl ester(461044-94-0)
    11. EPA Substance Registry System: Acetic acid (1S,2S)-2-benzyloxy-1-bromomethyl-2-(diethoxy-phosphoryl)-ethyl ester(461044-94-0)

  • 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: 461044-94-0(Hazardous Substances Data)

461044-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 461044-94-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,1,0,4 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 461044-94:
(8*4)+(7*6)+(6*1)+(5*0)+(4*4)+(3*4)+(2*9)+(1*4)=130
130 % 10 = 0
So 461044-94-0 is a valid CAS Registry Number.

461044-94-0Relevant articles and documents

Synthesis of diethyl (1R,2R)- and (1S,2R)-3-acetamido-1,2-dihydroxypropylphosphonates

Wroblewski, Andrzej E.,Balcerzak, Katarzyna B.

, p. 845 - 850 (2002)

Diastereomeric diethyl (1R,2R)- and (1S,2R)-2,3-epoxy-1-benzyloxypropylphosphonates were obtained from the respective 2,3-O-cyclohexylidene-1-hydroxypropylphosphonates via the following sequence of reactions: benzylation, acetal hydrolysis and transformation of the terminal diol into the epoxide using the Sharpless protocol. These epoxides were regioselectively opened with dibenzylamine to afford the title compounds after acetylation and hydrogenolysis.

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