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1332709-02-0

N,N-diethyl-2-phenyl-2-(2,4,6-trimethoxyphenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1332709-02-0 Structure

  • Basic information

    1. Product Name: N,N-diethyl-2-phenyl-2-(2,4,6-trimethoxyphenyl)acetamide
    2. Synonyms: N,N-diethyl-2-phenyl-2-(2,4,6-trimethoxyphenyl)acetamide
    3. CAS NO:1332709-02-0
    4. Molecular Formula:
    5. Molecular Weight: 357.45
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1332709-02-0.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,N-diethyl-2-phenyl-2-(2,4,6-trimethoxyphenyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-diethyl-2-phenyl-2-(2,4,6-trimethoxyphenyl)acetamide(1332709-02-0)
    11. EPA Substance Registry System: N,N-diethyl-2-phenyl-2-(2,4,6-trimethoxyphenyl)acetamide(1332709-02-0)

  • 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: 1332709-02-0(Hazardous Substances Data)

1332709-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332709-02-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,7,0 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1332709-02:
(9*1)+(8*3)+(7*3)+(6*2)+(5*7)+(4*0)+(3*9)+(2*0)+(1*2)=130
130 % 10 = 0
So 1332709-02-0 is a valid CAS Registry Number.

1332709-02-0Downstream Products

1332709-02-0Relevant articles and documents

Carbon-carbon bond-forming reactions of α-carbonyl carbocations: Exploration of a reversed-polarity equivalent of enolate chemistry

Lai, Ping-Shan,Dubland, Joshua A.,Sarwar, Mohammed G.,Chudzinski, Michael G.,Taylor, Mark S.

supporting information; experimental part, p. 7586 - 7592 (2011/10/12)

Carbon-carbon bond-forming reactions of putative α-carbonyl carbocation intermediates generated by Lewis acid- or silver-promoted ionizations of toluenesulfonate or halide leaving groups are described. This under-exploited mode of reactivity represents an 'umpolung' of conventional enolate chemistry, and enables C-C bond construction in both intra- and intermolecular contexts. Attempts to develop diastereoselective variants of this process using chiral ester and oxazolidinone-based auxiliaries are discussed.

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