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CAS

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1394131-96-4

(6S,7R)-6-hydroxy-7-(4-methoxyphenyl)-8-nitro-4-oxooctyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1394131-96-4 Structure

  • Basic information

    1. Product Name: (6S,7R)-6-hydroxy-7-(4-methoxyphenyl)-8-nitro-4-oxooctyl acetate
    2. Synonyms: (6S,7R)-6-hydroxy-7-(4-methoxyphenyl)-8-nitro-4-oxooctyl acetate
    3. CAS NO:1394131-96-4
    4. Molecular Formula:
    5. Molecular Weight: 353.372
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1394131-96-4.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: (6S,7R)-6-hydroxy-7-(4-methoxyphenyl)-8-nitro-4-oxooctyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (6S,7R)-6-hydroxy-7-(4-methoxyphenyl)-8-nitro-4-oxooctyl acetate(1394131-96-4)
    11. EPA Substance Registry System: (6S,7R)-6-hydroxy-7-(4-methoxyphenyl)-8-nitro-4-oxooctyl acetate(1394131-96-4)

  • 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: 1394131-96-4(Hazardous Substances Data)

1394131-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394131-96-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,1,3 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1394131-96:
(9*1)+(8*3)+(7*9)+(6*4)+(5*1)+(4*3)+(3*1)+(2*9)+(1*6)=164
164 % 10 = 4
So 1394131-96-4 is a valid CAS Registry Number.

1394131-96-4Relevant articles and documents

Enantioselective approach to functionalized quinolizidines: Synthesis of (+)-julandine and (+)-cryptopleurine

Pansare, Sunil V.,Dyapa, Rajendar

, p. 6776 - 6784 (2012/09/22)

An efficient synthesis of functionalized quinolizidines was developed from an enantiomerically enriched γ-nitroketone, which is easily prepared by an organocatalytic ketone-nitroalkene Michael addition. Oxidative ring expansion of the nitroketone followed

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