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1301608-49-0

N-Boc-O-Bn-seryl-phenylalanyl-alanyl-5-hydroxypentylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1301608-49-0 Structure

  • Basic information

    1. Product Name: N-Boc-O-Bn-seryl-phenylalanyl-alanyl-5-hydroxypentylamide
    2. Synonyms: N-Boc-O-Bn-seryl-phenylalanyl-alanyl-5-hydroxypentylamide
    3. CAS NO:1301608-49-0
    4. Molecular Formula:
    5. Molecular Weight: 598.74
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1301608-49-0.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: N-Boc-O-Bn-seryl-phenylalanyl-alanyl-5-hydroxypentylamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Boc-O-Bn-seryl-phenylalanyl-alanyl-5-hydroxypentylamide(1301608-49-0)
    11. EPA Substance Registry System: N-Boc-O-Bn-seryl-phenylalanyl-alanyl-5-hydroxypentylamide(1301608-49-0)

  • 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: 1301608-49-0(Hazardous Substances Data)

1301608-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1301608-49-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,1,6,0 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1301608-49:
(9*1)+(8*3)+(7*0)+(6*1)+(5*6)+(4*0)+(3*8)+(2*4)+(1*9)=110
110 % 10 = 0
So 1301608-49-0 is a valid CAS Registry Number.

1301608-49-0Relevant articles and documents

Carboaminoxylation as a tool to prepare functionalized polymeric materials: Introduction of biologically important residues by metal-free radical C-C coupling reactions

Lindner, Jean-Pierre,Studer, Armido

, p. 4090 - 4094 (2011/06/26)

Making a radical change! Radical C-C bond formation by thermal carboaminoxylation of alkoxyamines was used for functionalization of unsaturated macromolecular systems with biologically important residues (R; see scheme). The synthesized dendritic mannose-containing glycopolymers show very strong inhibition of the lectin Concanavalin A as measured by an enzyme-linked lectin assay. Copyright

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