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1393605-02-1

N-benzyloxycarbonyl-L-phenylalanine (7-methoxy-2-thioxobenzopyran-4-yl)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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  • 1393605-02-1 Structure

  • Basic information

    1. Product Name: N-benzyloxycarbonyl-L-phenylalanine (7-methoxy-2-thioxobenzopyran-4-yl)methyl ester
    2. Synonyms: N-benzyloxycarbonyl-L-phenylalanine (7-methoxy-2-thioxobenzopyran-4-yl)methyl ester
    3. CAS NO:1393605-02-1
    4. Molecular Formula:
    5. Molecular Weight: 503.576
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393605-02-1.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-benzyloxycarbonyl-L-phenylalanine (7-methoxy-2-thioxobenzopyran-4-yl)methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyloxycarbonyl-L-phenylalanine (7-methoxy-2-thioxobenzopyran-4-yl)methyl ester(1393605-02-1)
    11. EPA Substance Registry System: N-benzyloxycarbonyl-L-phenylalanine (7-methoxy-2-thioxobenzopyran-4-yl)methyl ester(1393605-02-1)

  • 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: 1393605-02-1(Hazardous Substances Data)

1393605-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393605-02-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,6,0 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1393605-02:
(9*1)+(8*3)+(7*9)+(6*3)+(5*6)+(4*0)+(3*5)+(2*0)+(1*2)=161
161 % 10 = 1
So 1393605-02-1 is a valid CAS Registry Number.

1393605-02-1Downstream Products

1393605-02-1Relevant articles and documents

Thionated coumarins and quinolones in the light triggered release of a model amino acid: Synthesis and photolysis studies

Fonseca, Andrea S.C.,Soares, Ana M.S.,Gon?alves, M. Sameiro T.,Costa, Susana P.G.

, p. 7892 - 7900 (2012/10/08)

Model amino acid ester conjugates bearing heterocycles with a thiocarbonyl group (thiocoumarins and thioquinolones) were prepared by a thionation reaction of the corresponding carbonyl precursors, with the aim of obtaining conjugates with higher photosensitivity at longer wavelengths. Photolysis studies were carried out under irradiation at different wavelengths in a photochemical reactor (250, 300, 350 and 419 nm), and it was found that the ester bond between the heterocycle and the model amino acid in the thionated analogues cleaved readily with shorter irradiation times than those of the corresponding precursors. Moreover, fast photolysis at 419 nm for thioquinolone ester conjugates (within minutes) was particularly interesting and the fact that some of the reported heterocycles displayed very different irradiation times, may provide the possibility for selective removal of one group in the presence of another photocleavable group. The (quinolin-2-thione-4-yl) methyl group may be considered as a new and very effective addition to the family of photocleavable protecting groups for carboxylic acids.

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