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CAS

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148516-49-8

2-(2-Benzoylamino-acetylamino)-3,3,3-trifluoro-2-hydroxy-propionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148516-49-8 Structure

  • Basic information

    1. Product Name: 2-(2-Benzoylamino-acetylamino)-3,3,3-trifluoro-2-hydroxy-propionic acid methyl ester
    2. Synonyms:
    3. CAS NO:148516-49-8
    4. Molecular Formula:
    5. Molecular Weight: 334.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148516-49-8.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-Benzoylamino-acetylamino)-3,3,3-trifluoro-2-hydroxy-propionic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-Benzoylamino-acetylamino)-3,3,3-trifluoro-2-hydroxy-propionic acid methyl ester(148516-49-8)
    11. EPA Substance Registry System: 2-(2-Benzoylamino-acetylamino)-3,3,3-trifluoro-2-hydroxy-propionic acid methyl ester(148516-49-8)

  • 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: 148516-49-8(Hazardous Substances Data)

148516-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148516-49-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,5,1 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 148516-49:
(8*1)+(7*4)+(6*8)+(5*5)+(4*1)+(3*6)+(2*4)+(1*9)=148
148 % 10 = 8
So 148516-49-8 is a valid CAS Registry Number.

148516-49-8Downstream Products

148516-49-8Relevant articles and documents

Peptide modification by incorporation of α-trifluoromethyl α-amino acids via trifluoromethyl-substituted acylimines

Hoess, E.,Rudolph, M.,Seymour, L.,Schierlinger, C.,Burger, K.

, p. 163 - 170 (1993)

α-Trifluoromethyl-substituted α-amino acids can be introduced into the C-terminal position of peptides via acylimines obtained on reaction of trifluoropyruvates with N-protected α-amino acid amides and dipeptide amides, respectively.

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