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CAS

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120566-72-5

(S)-3-<2-(Acetyloxy)-1-phenylethyl>-6-methyl-3,6-diazabicyclo<3.1.0>hexane-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 120566-72-5 Structure

  • Basic information

    1. Product Name: (S)-3-<2-(Acetyloxy)-1-phenylethyl>-6-methyl-3,6-diazabicyclo<3.1.0>hexane-2,4-dione
    2. Synonyms: (S)-3-<2-(Acetyloxy)-1-phenylethyl>-6-methyl-3,6-diazabicyclo<3.1.0>hexane-2,4-dione
    3. CAS NO:120566-72-5
    4. Molecular Formula:
    5. Molecular Weight: 288.303
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120566-72-5.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: (S)-3-<2-(Acetyloxy)-1-phenylethyl>-6-methyl-3,6-diazabicyclo<3.1.0>hexane-2,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-<2-(Acetyloxy)-1-phenylethyl>-6-methyl-3,6-diazabicyclo<3.1.0>hexane-2,4-dione(120566-72-5)
    11. EPA Substance Registry System: (S)-3-<2-(Acetyloxy)-1-phenylethyl>-6-methyl-3,6-diazabicyclo<3.1.0>hexane-2,4-dione(120566-72-5)

  • 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: 120566-72-5(Hazardous Substances Data)

120566-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120566-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,6 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120566-72:
(8*1)+(7*2)+(6*0)+(5*5)+(4*6)+(3*6)+(2*7)+(1*2)=105
105 % 10 = 5
So 120566-72-5 is a valid CAS Registry Number.

120566-72-5Relevant articles and documents

An Approach to the 3,8-Diazabicyclooctane Moiety of Naphthyridinomycin and Quinocarcin via 1,3-Dipolar Cycloaddition of Photochemically Generated Azomethine Ylides.

Garner, Philip,Sunitha, K.,Shanthilal, T.

, p. 3525 - 3528 (2007/10/02)

An attractive strategy for construction of the 3,8-diazabicyclooctane moiety of targets 1 and 2 involving the 1,3-dipolar cycloaddition of photochemical generated azomethine ylides is presented.

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