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CAS

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156025-77-3

N-(triflyloxy)-N-methylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 156025-77-3 Structure

  • Basic information

    1. Product Name: N-(triflyloxy)-N-methylbenzamide
    2. Synonyms: N-(triflyloxy)-N-methylbenzamide
    3. CAS NO:156025-77-3
    4. Molecular Formula:
    5. Molecular Weight: 283.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 156025-77-3.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: N-(triflyloxy)-N-methylbenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(triflyloxy)-N-methylbenzamide(156025-77-3)
    11. EPA Substance Registry System: N-(triflyloxy)-N-methylbenzamide(156025-77-3)

  • 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: 156025-77-3(Hazardous Substances Data)

156025-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156025-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,0,2 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 156025-77:
(8*1)+(7*5)+(6*6)+(5*0)+(4*2)+(3*5)+(2*7)+(1*7)=123
123 % 10 = 3
So 156025-77-3 is a valid CAS Registry Number.

156025-77-3Relevant articles and documents

Generation of N-Acyl Iminium Ions from Ionization-Rearrangement Reactions of N-Triflyloxy Amides

Hoffman, Robert V.,Nayyar, Naresh K.,Shankweiler, Jean M.,Klinekole III, Bruce W.

, p. 3231 - 3234 (2007/10/02)

N-Triflyloxy amides undergo ionization in refluxing isopropanol to give N-acyliminium ions which can be trapped by addition of allyltrimethylsilane to the reaction mixture.Alternatively they can be converted to N-(isopropoxy)alkyl amides and then back to

A Facile Preparation of N-(Isopropoxyalkyl) Amides by Generation and Trapping of N-Acyliminium Ions from Ionization-Rearrangement Reactions of N-Triflyloxy Amides

Hoffman, Robert V.,Nayyar, Naresh K.

, p. 3530 - 3539 (2007/10/02)

A series of hydroxamic acids were converted to N-triflyloxy amides which were heated in 2-propanol to give N-(1-isopropoxyalkyl) amides in high yields.The method is simple, direct, and extremely tolerant of structural diversity both in the N-acyl group, a

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