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CAS

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478932-16-0

2-(2-phenoxypropionylamino)acrylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 478932-16-0 Structure

  • Basic information

    1. Product Name: 2-(2-phenoxypropionylamino)acrylic acid
    2. Synonyms: 2-(2-phenoxypropionylamino)acrylic acid
    3. CAS NO:478932-16-0
    4. Molecular Formula:
    5. Molecular Weight: 235.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 478932-16-0.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: 2-(2-phenoxypropionylamino)acrylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-phenoxypropionylamino)acrylic acid(478932-16-0)
    11. EPA Substance Registry System: 2-(2-phenoxypropionylamino)acrylic acid(478932-16-0)

  • 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: 478932-16-0(Hazardous Substances Data)

478932-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478932-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,9,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 478932-16:
(8*4)+(7*7)+(6*8)+(5*9)+(4*3)+(3*2)+(2*1)+(1*6)=200
200 % 10 = 0
So 478932-16-0 is a valid CAS Registry Number.

478932-16-0Relevant articles and documents

Mild method for cleavage of dehydroalanine units: Highly efficient conversion of nocathiacin I to nocathiacin IV

Regueiro-Ren, Alicia,Ueda, Yasutsugu

, p. 8699 - 8702 (2007/10/03)

Thiazolyl peptide antibacterial nocathiacin I (1) was converted to nocathiacin IV (4) in high yield using iodomethane and hydriodic acid in THF at 45 °C. Several simplified dehydroalanine-containing systems undergo dehydroalanine cleavage under the same conditions, although in these cases iodomethane is not needed for efficient conversion. The mild reaction conditions are in contrast with other methods described in the literature.

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