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CAS

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951167-20-7

(5R)-7-[(1S)-1-phenylethyl]-1,7-diazaspiro[4.4]nonane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 951167-20-7 Structure

  • Basic information

    1. Product Name: (5R)-7-[(1S)-1-phenylethyl]-1,7-diazaspiro[4.4]nonane
    2. Synonyms: (5R)-7-[(1S)-1-Phenylethyl]-1,7-diazaspiro[4.4]nonan
    3. CAS NO:951167-20-7
    4. Molecular Formula: C15H22N2
    5. Molecular Weight: 230.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 951167-20-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 332.5°C at 760 mmHg
    3. Flash Point: 127.8°C
    4. Appearance: N/A
    5. Density: 1.06g/cm3
    6. Vapor Pressure: 0.000145mmHg at 25°C
    7. Refractive Index: 1.581
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (5R)-7-[(1S)-1-phenylethyl]-1,7-diazaspiro[4.4]nonane(CAS DataBase Reference)
    11. NIST Chemistry Reference: (5R)-7-[(1S)-1-phenylethyl]-1,7-diazaspiro[4.4]nonane(951167-20-7)
    12. EPA Substance Registry System: (5R)-7-[(1S)-1-phenylethyl]-1,7-diazaspiro[4.4]nonane(951167-20-7)

  • 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: 951167-20-7(Hazardous Substances Data)

951167-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 951167-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,1,6 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 951167-20:
(8*9)+(7*5)+(6*1)+(5*1)+(4*6)+(3*7)+(2*2)+(1*0)=167
167 % 10 = 7
So 951167-20-7 is a valid CAS Registry Number.

951167-20-7Downstream Products

951167-20-7Relevant articles and documents

Spirobicyclic diamines. Part 3: Synthesis and metal complexation of proline-derived [4.4]-spirodiamines

Kelleher, Fintan,Kelly, Sinead,McKee, Vickie

, p. 9235 - 9242 (2007)

The syntheses of racemic and homochiral [4.4]-spirolactams, starting from l-proline, in good yields are described. Reduction of the lactam carbonyl group of spirolactams, containing chiral substituents on the lactam nitrogen, with lithium aluminium hydride, gives?a series of homochiral [4.4]-spirodiamines. The crystal structure of one of these spirodiamines on complexation with zinc chloride was obtained. Interestingly it showed a hydrogen-bonded dimeric structure, where the monomers are diastereoisomeric diamines.

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