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CAS

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741716-58-5

2-[phenyl-(2,2,2-trichloro-acetylcarbamoyloxy)-methyl]-acrylic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 741716-58-5 Structure

  • Basic information

    1. Product Name: 2-[phenyl-(2,2,2-trichloro-acetylcarbamoyloxy)-methyl]-acrylic acid tert-butyl ester
    2. Synonyms: 2-[phenyl-(2,2,2-trichloro-acetylcarbamoyloxy)-methyl]-acrylic acid tert-butyl ester
    3. CAS NO:741716-58-5
    4. Molecular Formula:
    5. Molecular Weight: 422.693
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 741716-58-5.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-[phenyl-(2,2,2-trichloro-acetylcarbamoyloxy)-methyl]-acrylic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[phenyl-(2,2,2-trichloro-acetylcarbamoyloxy)-methyl]-acrylic acid tert-butyl ester(741716-58-5)
    11. EPA Substance Registry System: 2-[phenyl-(2,2,2-trichloro-acetylcarbamoyloxy)-methyl]-acrylic acid tert-butyl ester(741716-58-5)

  • 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: 741716-58-5(Hazardous Substances Data)

741716-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 741716-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,7,1 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 741716-58:
(8*7)+(7*4)+(6*1)+(5*7)+(4*1)+(3*6)+(2*5)+(1*8)=165
165 % 10 = 5
So 741716-58-5 is a valid CAS Registry Number.

741716-58-5Relevant articles and documents

Asymmetric organocatalysed [1,3]-sigmatropic rearrangements

Kobbelgaard, Sara,Brandes, Sebastian,Jorgensen, Karl Anker

experimental part, p. 1464 - 1471 (2009/04/04)

The first organocatalysed enantioselective [1,3]-sigmatropic O- to N-rearrangement reactions are presented. The reactions take place under regio- and enantioselective control, and are catalysed by cinchona alkaloids. Two reactions have been developed the first one is the rearrangement of imidates to amides, while the other rear rangement occurs from carbamates to amines via a decarboxylation. Both transformations give nitrogen protected β-amino acid derivatives as the product. These novel asymmetric organocatalysed [1,3]-sigmatropic O- to N-rearrangement reactions provide a reliable and efficient synthetic method for obtaining enantioenriched β-amino acid derivates in good yield from racemic starting materials.

Stereoselective iodocyclization of 3-acylamino-2-methylene alkanoates: Synthesis of analogues of N-benzoyl-syn-phenylisoserine

Galeazzi, Roberta,Martelli, Gianluca,Mobbili, Giovanna,Orena, Mario,Rinaldi, Samuele

, p. 2571 - 2574 (2007/10/03)

(Matrix Presented) A convenient approach to racemic analogues of N-benzoyl-syn-phenylisoserine was realized via the stereoselective iodocyclization of amides obtained from Baylis-Hillman adducts.

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