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2-[(tert- Butyloxycarbonyl) Aminooxy]-N(2- Aminoethyl)Acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160818-51-9 Structure
  • Basic information

    1. Product Name: 2-[(tert- Butyloxycarbonyl) Aminooxy]-N(2- Aminoethyl)Acetamide
    2. Synonyms:
    3. CAS NO:160818-51-9
    4. Molecular Formula:
    5. Molecular Weight: 233.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160818-51-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.135±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[(tert- Butyloxycarbonyl) Aminooxy]-N(2- Aminoethyl)Acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(tert- Butyloxycarbonyl) Aminooxy]-N(2- Aminoethyl)Acetamide(160818-51-9)
    11. EPA Substance Registry System: 2-[(tert- Butyloxycarbonyl) Aminooxy]-N(2- Aminoethyl)Acetamide(160818-51-9)
  • 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: 160818-51-9(Hazardous Substances Data)

160818-51-9 Usage

Molecular weight

246.3

Appearance

White crystalline solid

Solubility

Soluble in water and common organic solvents such as ethanol, methanol, and DMSO

Functional groups

tert-Butyloxycarbonyl (Boc), aminooxy, and aminoethyl

Use

As a reagent in the synthesis of peptide-based drugs and as a building block in the creation of bioconjugates

Property

Protects amino groups in the presence of other reactive functional groups

Potential application

In the treatment of various diseases, including cancer and neurodegenerative disorders, due to its ability to target specific biomolecules and pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 160818-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,8,1 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 160818-51:
(8*1)+(7*6)+(6*0)+(5*8)+(4*1)+(3*8)+(2*5)+(1*1)=129
129 % 10 = 9
So 160818-51-9 is a valid CAS Registry Number.

160818-51-9Downstream Products

160818-51-9Relevant articles and documents

Synthesis of an enlarged library of dynamic DNA activators with oxime, disulfide and hydrazone bridges

Montenegro, Javier,Bang, Eun-Kyoung,Sakai, Naomi,Matile, Stefan

, p. 10436 - 10443 (2012/10/18)

Dynamic amphiphiles have a bridge between their charged head and their hydrophobic tails. The presence of dynamic covalent bonds is of interest for differential and biosensing applications as well as for rapid access to the libraries needed to screen for gene delivery or cellular uptake of siRNA. However, efforts to develop libraries have so far concentrated on hydrazone bridges to monocationic heads. Here, we report synthesis efforts to enlarge this focused library with oxime and disulfide bridges and dynamic amphiphiles with more than one positive charge. Evaluation in fluorogenic vesicles reveals best activation of DNA as ion transporters by dynamic amphiphiles with dendritic scaffolds, doubly charged heads and four tails. Moreover, oximes, contrary to hydrazones, remain active under acidic conditions. Linear elongation of dendritic head-groups seems to cause increasing detergent effects and should therefore be avoided. Head on: Design, synthesis and evaluation of dynamic amphiphiles with singly or doubly charged peptide dendrons as head-groups; hydrazones, oximes and disulfides as bridges; and with fragrant tails are reported. Amphiphiles with two charges and four tails (see figure) are identified as the most powerful activators of DNA as ion transporters and thus as the most promising family to screen for gene and siRNA delivery. Copyright

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