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CAS

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231617-03-1

N-[1-(2,5-dimethoxy-phenyl)-ethyl]-N-(1-phenyl-but-3-enyl)-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 231617-03-1 Structure

  • Basic information

    1. Product Name: N-[1-(2,5-dimethoxy-phenyl)-ethyl]-N-(1-phenyl-but-3-enyl)-acetamide
    2. Synonyms:
    3. CAS NO:231617-03-1
    4. Molecular Formula:
    5. Molecular Weight: 353.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 231617-03-1.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: N-[1-(2,5-dimethoxy-phenyl)-ethyl]-N-(1-phenyl-but-3-enyl)-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[1-(2,5-dimethoxy-phenyl)-ethyl]-N-(1-phenyl-but-3-enyl)-acetamide(231617-03-1)
    11. EPA Substance Registry System: N-[1-(2,5-dimethoxy-phenyl)-ethyl]-N-(1-phenyl-but-3-enyl)-acetamide(231617-03-1)

  • 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: 231617-03-1(Hazardous Substances Data)

231617-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 231617-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,1,6,1 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 231617-03:
(8*2)+(7*3)+(6*1)+(5*6)+(4*1)+(3*7)+(2*0)+(1*3)=101
101 % 10 = 1
So 231617-03-1 is a valid CAS Registry Number.

231617-03-1Relevant articles and documents

Design, synthesis, and optical resolution of a novel non-natural chiral auxiliary, 1-(2,5-dimethoxyphenyl)ethylamine. Application to diastereoselective alkylation of aldimines

Kohara, Takehiro,Hashimoto, Yukihiko,Saigo, Kazuhiko

, p. 6453 - 6464 (2007/10/03)

A chiral amine; 1-(2,5-dimethoxyphenyl)ethylamine, was found to be an effective chiral auxiliary for the diastereoselective alkylation of its aldimines with alkylmetals. The 1-(2,5-dimethoxyphenyl)ethyl group of the chiral auxiliary could be removed by the acetylation and then oxidation of the resultant alkylated product, accompanying an amino-transfer from the chiral auxiliary to the final product. Racemic 1-(2,5- dimethoxyphenyl)ethylamine could be easily synthesized from 1,4- dimethoxybenzene and resolved by the diastereomeric salt formation with mandelic acid to give both enantiomers in pure forms.

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