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CAS

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134253-04-6

1-((1R,5S)-3-Benzyl-3,6-diaza-bicyclo[3.2.0]hept-6-yl)-2,2,2-trifluoro-ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134253-04-6 Structure

  • Basic information

    1. Product Name: 1-((1R,5S)-3-Benzyl-3,6-diaza-bicyclo[3.2.0]hept-6-yl)-2,2,2-trifluoro-ethanone
    2. Synonyms: 1-((1R,5S)-3-Benzyl-3,6-diaza-bicyclo[3.2.0]hept-6-yl)-2,2,2-trifluoro-ethanone
    3. CAS NO:134253-04-6
    4. Molecular Formula:
    5. Molecular Weight: 284.281
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134253-04-6.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: 1-((1R,5S)-3-Benzyl-3,6-diaza-bicyclo[3.2.0]hept-6-yl)-2,2,2-trifluoro-ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-((1R,5S)-3-Benzyl-3,6-diaza-bicyclo[3.2.0]hept-6-yl)-2,2,2-trifluoro-ethanone(134253-04-6)
    11. EPA Substance Registry System: 1-((1R,5S)-3-Benzyl-3,6-diaza-bicyclo[3.2.0]hept-6-yl)-2,2,2-trifluoro-ethanone(134253-04-6)

  • 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: 134253-04-6(Hazardous Substances Data)

134253-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134253-04-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,5 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 134253-04:
(8*1)+(7*3)+(6*4)+(5*2)+(4*5)+(3*3)+(2*0)+(1*4)=96
96 % 10 = 6
So 134253-04-6 is a valid CAS Registry Number.

134253-04-6Relevant articles and documents

Synthesis of a new bridged diamine 3,6-diazabicyclo [3.2.0] heptane: Applications to the synthesis of quinolone antibacterials

Jacquet,Bouzard,Kiechel,Remuzon

, p. 1565 - 1568 (2007/10/02)

Diprotected 3,6-diazabicyclo [3.2.0] heptane has been prepared by an highly efficient process. Selective deprotection, followed by condensation with 7-halogenoquinolones led to the naphthyridones 10 and 13 and the quinolone 14.

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