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CAS

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1318074-46-2

2-acetoxy-N-benzyl-N-(3-methoxyphenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1318074-46-2 Structure

  • Basic information

    1. Product Name: 2-acetoxy-N-benzyl-N-(3-methoxyphenyl)acetamide
    2. Synonyms: 2-acetoxy-N-benzyl-N-(3-methoxyphenyl)acetamide
    3. CAS NO:1318074-46-2
    4. Molecular Formula:
    5. Molecular Weight: 313.353
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1318074-46-2.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: 2-acetoxy-N-benzyl-N-(3-methoxyphenyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-acetoxy-N-benzyl-N-(3-methoxyphenyl)acetamide(1318074-46-2)
    11. EPA Substance Registry System: 2-acetoxy-N-benzyl-N-(3-methoxyphenyl)acetamide(1318074-46-2)

  • 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: 1318074-46-2(Hazardous Substances Data)

1318074-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1318074-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,8,0,7 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1318074-46:
(9*1)+(8*3)+(7*1)+(6*8)+(5*0)+(4*7)+(3*4)+(2*4)+(1*6)=142
142 % 10 = 2
So 1318074-46-2 is a valid CAS Registry Number.

1318074-46-2Relevant articles and documents

Exploiting Sm(ii) and Sm(iii) in SmI2-initiated reaction cascades: Application in a tag removal-cyclisation approach to spirooxindole scaffolds

Coote, Susannah C.,Quenum, Seidjolo,Procter, David J.

supporting information; experimental part, p. 5104 - 5108 (2011/08/07)

A tag removal-cyclisation sequence is described that is initiated by reduction using a Sm(ii) species and completed by a Sm(iii) Lewis acid that is formed in an earlier stage. Therefore, the reaction cascade utilises both oxidation states of a samarium reagent in discrete steps and allows access to privileged, pyrrolidinyl-spirooxindole scaffolds and analogues inspired by the anti-cancer natural product spirotryprostatin A. The Royal Society of Chemistry 2011.

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