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1301743-46-3

(7S)-7-[(1R)-1-(4-methoxyphenyl)-2-nitroethyl]-1,4-dioxaspiro[4.5]decan-8-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1301743-46-3 Structure

  • Basic information

    1. Product Name: (7S)-7-[(1R)-1-(4-methoxyphenyl)-2-nitroethyl]-1,4-dioxaspiro[4.5]decan-8-one
    2. Synonyms: (7S)-7-[(1R)-1-(4-methoxyphenyl)-2-nitroethyl]-1,4-dioxaspiro[4.5]decan-8-one
    3. CAS NO:1301743-46-3
    4. Molecular Formula:
    5. Molecular Weight: 335.357
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1301743-46-3.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: (7S)-7-[(1R)-1-(4-methoxyphenyl)-2-nitroethyl]-1,4-dioxaspiro[4.5]decan-8-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (7S)-7-[(1R)-1-(4-methoxyphenyl)-2-nitroethyl]-1,4-dioxaspiro[4.5]decan-8-one(1301743-46-3)
    11. EPA Substance Registry System: (7S)-7-[(1R)-1-(4-methoxyphenyl)-2-nitroethyl]-1,4-dioxaspiro[4.5]decan-8-one(1301743-46-3)

  • 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: 1301743-46-3(Hazardous Substances Data)

1301743-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1301743-46-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,1,7,4 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1301743-46:
(9*1)+(8*3)+(7*0)+(6*1)+(5*7)+(4*4)+(3*3)+(2*4)+(1*6)=113
113 % 10 = 3
So 1301743-46-3 is a valid CAS Registry Number.

1301743-46-3Relevant articles and documents

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

Pansare, Sunil V.,Dyapa, Rajendar

, p. 6776 - 6784 (2012)

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

A simple enantioselective route to functionalized indolizidines: Synthesis of (+)-ipalbidine and (+)-antofine

Pansare, Sunil V.,Lingampally, Rajinikanth,Dyapa, Rajendar

supporting information; experimental part, p. 2235 - 2238 (2011/06/19)

An efficient route to functionalized indolizidines from an enantiomerically enriched γ-nitro ketone is described. The nitro ketone is obtained by an organocatalytic, enantioselective ketone-nitro alkene Michael addition. Oxidative ring expansion of the ni

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