Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1360138-56-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1360138-56-2 Structure
  • Basic information

    1. Product Name: (15)N-(S)-1-benzyl-3-(3-methyl-1-(3-methylureido)butan-2-yl)urea
    2. Synonyms:
    3. CAS NO:1360138-56-2
    4. Molecular Formula:
    5. Molecular Weight: 293.374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1360138-56-2.mol
    9. Article Data: 1
  • 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: (15)N-(S)-1-benzyl-3-(3-methyl-1-(3-methylureido)butan-2-yl)urea(CAS DataBase Reference)
    10. NIST Chemistry Reference: (15)N-(S)-1-benzyl-3-(3-methyl-1-(3-methylureido)butan-2-yl)urea(1360138-56-2)
    11. EPA Substance Registry System: (15)N-(S)-1-benzyl-3-(3-methyl-1-(3-methylureido)butan-2-yl)urea(1360138-56-2)
  • 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: 1360138-56-2(Hazardous Substances Data)

1360138-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1360138-56-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,1,3 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1360138-56:
(9*1)+(8*3)+(7*6)+(6*0)+(5*1)+(4*3)+(3*8)+(2*5)+(1*6)=132
132 % 10 = 2
So 1360138-56-2 is a valid CAS Registry Number.

1360138-56-2Downstream Products

1360138-56-2Relevant articles and documents

Solid state NMR studies of oligourea foldamers: Interaction of 15N-labelled amphiphilic helices with oriented lipid membranes

Aisenbrey, Christopher,Pendem, Nagendar,Guichard, Gilles,Bechinger, Burkhard

, p. 1440 - 1447 (2012/04/10)

Synthetic oligomers that are derived from natural polypeptide sequences, albeit with unnatural building blocks, have attracted considerable interest in mimicking bioactive peptides and proteins. Many of those compounds adopt stable folds in aqueous environments that resemble protein structural elements. Here we have chemically prepared aliphatic oligoureas and labeled them at selected positions with 15N for structural investigations using solid-state NMR spectroscopy. In the first step, the main tensor elements and the molecular alignment of the 15N chemical shift tensor were analyzed. This was possible by using a two-dimensional heteronuclear chemical shift/dipolar coupling correlation experiment on a model compound that represents the chemical, and thereby also the chemical shift characteristics, of the urea bond. In the next step 15N labeled versions of an amphipathic oligourea, that exert potent antimicrobial activities and that adopt stable helical structures in aqueous environments, were prepared. These compounds were reconstituted into oriented phospholipid bilayers and the 15N chemical shift and 1H-15N dipolar couplings of two labeled sites were determined by solid-state NMR spectroscopy. The data are indicative of an alignment of this helix parallel to the membrane surface in excellent agreement with the amphipathic character of the foldamer and consistent with previous models explaining the antimicrobial activities of α-peptides.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1360138-56-2