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545391-03-5

2-benzyloxycarbonylamino-thiopropionic acid S-(4-guanidino-phenyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 545391-03-5 Structure

  • Basic information

    1. Product Name: 2-benzyloxycarbonylamino-thiopropionic acid S-(4-guanidino-phenyl) ester
    2. Synonyms: 2-benzyloxycarbonylamino-thiopropionic acid S-(4-guanidino-phenyl) ester
    3. CAS NO:545391-03-5
    4. Molecular Formula:
    5. Molecular Weight: 372.448
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 545391-03-5.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-benzyloxycarbonylamino-thiopropionic acid S-(4-guanidino-phenyl) ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzyloxycarbonylamino-thiopropionic acid S-(4-guanidino-phenyl) ester(545391-03-5)
    11. EPA Substance Registry System: 2-benzyloxycarbonylamino-thiopropionic acid S-(4-guanidino-phenyl) ester(545391-03-5)

  • 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: 545391-03-5(Hazardous Substances Data)

545391-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 545391-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,5,3,9 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 545391-03:
(8*5)+(7*4)+(6*5)+(5*3)+(4*9)+(3*1)+(2*0)+(1*3)=155
155 % 10 = 5
So 545391-03-5 is a valid CAS Registry Number.

545391-03-5Downstream Products

545391-03-5Relevant articles and documents

Reverse proteolysis promoted by in situ generated peptide ester fragments

Wehofsky, Nicole,Koglin, Norman,Thust, Sven,Bordusa, Frank

, p. 6126 - 6133 (2007/10/03)

In this contribution we describe a general synthesis concept for the in situ preparation of protease specific reactants using methyl thioesters as universal precursors. The precursor esters are readily available by standard synthesis procedures and can be

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