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1334521-44-6

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  • 1334521-44-6 Structure

  • Basic information

    1. Product Name: SS-((2R,3R)-3-benzamido-4-oxoazetidin-2-yl)O-methyl carbon(dithioperoxoate)
    2. Synonyms: SS-((2R,3R)-3-benzamido-4-oxoazetidin-2-yl)O-methyl carbon(dithioperoxoate)
    3. CAS NO:1334521-44-6
    4. Molecular Formula:
    5. Molecular Weight: 312.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1334521-44-6.mol
    9. Article Data: 1

  • 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: SS-((2R,3R)-3-benzamido-4-oxoazetidin-2-yl)O-methyl carbon(dithioperoxoate)(CAS DataBase Reference)
    10. NIST Chemistry Reference: SS-((2R,3R)-3-benzamido-4-oxoazetidin-2-yl)O-methyl carbon(dithioperoxoate)(1334521-44-6)
    11. EPA Substance Registry System: SS-((2R,3R)-3-benzamido-4-oxoazetidin-2-yl)O-methyl carbon(dithioperoxoate)(1334521-44-6)

  • 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: 1334521-44-6(Hazardous Substances Data)

1334521-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1334521-44-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,5,2 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1334521-44:
(9*1)+(8*3)+(7*3)+(6*4)+(5*5)+(4*2)+(3*1)+(2*4)+(1*4)=126
126 % 10 = 6
So 1334521-44-6 is a valid CAS Registry Number.

1334521-44-6Downstream Products

1334521-44-6Relevant articles and documents

Asymmetric synthesis of monocyclic β-lactams from l-cysteine using photochemistry

Lu, Xiao,Long, Timothy E.

, p. 5051 - 5054 (2011/10/09)

An asymmetric method to synthesize cis-configured β-lactams using photochemistry has been developed. Aerobic photo-oxidation of l-cysteine-derived thiazolidine hydroxamate esters afforded C-3 hydroxylated products which when cyclized and deprotected gave

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