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C60H110O24S5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1245938-18-4 Structure
  • Basic information

    1. Product Name: C60H110O24S5
    2. Synonyms:
    3. CAS NO:1245938-18-4
    4. Molecular Formula:
    5. Molecular Weight: 1375.85
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1245938-18-4.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: C60H110O24S5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C60H110O24S5(1245938-18-4)
    11. EPA Substance Registry System: C60H110O24S5(1245938-18-4)
  • 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: 1245938-18-4(Hazardous Substances Data)

1245938-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1245938-18-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,9,3 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1245938-18:
(9*1)+(8*2)+(7*4)+(6*5)+(5*9)+(4*3)+(3*8)+(2*1)+(1*8)=174
174 % 10 = 4
So 1245938-18-4 is a valid CAS Registry Number.

1245938-18-4Downstream Products

1245938-18-4Relevant articles and documents

Novel synthetic LPDs consisting of different cholesterol derivatives for gene transfer into hepatocytes

Lu, Jiao,Zhu, Di,Zhang, Zhi-Rong,Hai, Li,Wu, Yong,Sun, Xun

, p. 520 - 535 (2011/12/02)

In the present study, LPDs composing of a series of novel synthetic cholesterylated derivatives bearing a cluster of galactose residues and different spacer lengths were prepared for performing target gene delivery to hepatocytes and their physiochemical properties as well as gene transfer efficiency were investigated. In agreement with the "clustering effect" known to occur with more complex oligomeric structures, the addition of galactose residues under optimized spatial arrangement condition invariably increased the transfect efficiency into hepatoma cells, which can be owed to the sufficient binding of galactose ligands to the ASGPR on hepatocytes. However, the gene transfer ability to hepatocytes was not always improved with extended spacer arms, suggesting a spatial binding sites arrangement of the receptor. Moreover, our research has established galactosylated LPDs, specifically, LPDIIb, LPDIIIc, and LPDIVe as potential vectors to deliver special genes into hepatocytes with low toxicity, combining the condensing effect of protamine and the targeting capability of cholesterylated thiogalactosides.

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