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156776-80-6

N-tert-butoxy-2-phenylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156776-80-6 Structure

  • Basic information

    1. Product Name: N-tert-butoxy-2-phenylacetamide
    2. Synonyms: N-tert-butoxy-2-phenylacetamide
    3. CAS NO:156776-80-6
    4. Molecular Formula:
    5. Molecular Weight: 207.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156776-80-6.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-tert-butoxy-2-phenylacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-tert-butoxy-2-phenylacetamide(156776-80-6)
    11. EPA Substance Registry System: N-tert-butoxy-2-phenylacetamide(156776-80-6)

  • 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: 156776-80-6(Hazardous Substances Data)

156776-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156776-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,7 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156776-80:
(8*1)+(7*5)+(6*6)+(5*7)+(4*7)+(3*6)+(2*8)+(1*0)=176
176 % 10 = 6
So 156776-80-6 is a valid CAS Registry Number.

156776-80-6Relevant articles and documents

A new synthesis of N-alkoxy-2-ethoxyarylacetamides from N-alkoxy-N-chloroarylacetamides with triethylamine in ethanol

Kikugawa,Shimada,Kato,Sakamoto

, p. 2192 - 2194 (1993)

Treatment of N-alkoxy-N-chloroarylacetamides with triethylamine in ethanol results in removal of a chlorine atom and introduction of an ethoxy group at the C-2 position of arylacetamides in moderate yields.

Copper-catalyzed cross-coupling of O -alkyl hydroxamates with aryl iodides

Kukosha, Tatyana,Trufilkina, Nadezhda,Belyakov, Sergey,Katkevics, Martins

, p. 2413 - 2423 (2012/09/07)

N-Aryl-O-alkylhydroxamic acid derivatives were prepared by copper-catalyzed cross-coupling of hydroxamates with aryl iodides. The reaction conditions are compatible with standard hydroxy-protecting groups on the hydroxylamine moiety and are applicable to

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