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90849-46-0

Acetic acid, [[2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinyl]oxy]-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 90849-46-0 Structure

  • Basic information

    1. Product Name: Acetic acid, [[2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinyl]oxy]-, (S)-
    2. Synonyms:
    3. CAS NO:90849-46-0
    4. Molecular Formula: C13H14N2O6
    5. Molecular Weight: 294.264
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90849-46-0.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, [[2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinyl]oxy]-, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid, [[2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinyl]oxy]-, (S)-(90849-46-0)
    11. EPA Substance Registry System: Acetic acid, [[2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinyl]oxy]-, (S)-(90849-46-0)

  • 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: 90849-46-0(Hazardous Substances Data)

90849-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90849-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,4 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90849-46:
(7*9)+(6*0)+(5*8)+(4*4)+(3*9)+(2*4)+(1*6)=160
160 % 10 = 0
So 90849-46-0 is a valid CAS Registry Number.

90849-46-0Downstream Products

90849-46-0Relevant articles and documents

Synthesis and Biological Activity of Substituted oxy>acetic Acids. A New Class of Heteroatom-Activated β-Lactam Antibiotics

Woulfe, Steven R.,Miller, Marvin J.

, p. 1447 - 1453 (2007/10/02)

The synthesis of substituted oxy>acetic acids (1) is described. 3--N-hydroxy-2-azetidinones (13a, b), prepared from serine and threonine, were alkylated with 2-(trimethylsilyl)ethyl bromoacetate

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