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  • 84828-82-0 Structure
  • Basic information

    1. Product Name: C42H75N5O21
    2. Synonyms:
    3. CAS NO:84828-82-0
    4. Molecular Formula:
    5. Molecular Weight: 986.078
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 84828-82-0.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: C42H75N5O21(CAS DataBase Reference)
    10. NIST Chemistry Reference: C42H75N5O21(84828-82-0)
    11. EPA Substance Registry System: C42H75N5O21(84828-82-0)
  • 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: 84828-82-0(Hazardous Substances Data)

84828-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84828-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,2 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 84828-82:
(7*8)+(6*4)+(5*8)+(4*2)+(3*8)+(2*8)+(1*2)=170
170 % 10 = 0
So 84828-82-0 is a valid CAS Registry Number.

84828-82-0Downstream Products

84828-82-0Relevant articles and documents

Synthesis of hyaluronan-amikacin conjugate and its bactericidal activity against intracellular bacteria in vitro and in vivo

Wang, Zhaojie,Qiu, Yuanhao,Hou, Chunyan,Wang, Dongdong,Sun, Feifei,Li, Xiaojun,Wang, Feng,Yi, Hong,Mu, Haibo,Duan, Jinyou

, p. 132 - 140 (2018)

Aminoglycosides are often subtherapeutic to intracellular infections due to their high hydrophilicity. Here we used hyaluronic acid (HA) as a carbohydrate carrier of the aminoglycoside antibiotic, amikacin (AM) to deal with intracellular bacterial infections. The hyaluronan-amikacin conjugate (HA-AM) was synthesized by ‘click’ reaction between HA-propargyl amide (HAPA) and AM-azide. This conjugate with little cytotoxicity retained antibiotic effects on planktonic bacteria and showed better intracellular bactericidal activity than the antibiotic did. In addition, this conjugate was more efficient in reducing bacteria burden in an in vivo acute infection model than amikacin did. These results suggested that hyaluronic acid conjugation could reduce the dosage of antibiotic in treatment of intracellular bacterial infection, and further helping to alleviate the emergence of drug resistance in bacteria due to a long-term, high-dosage treatment.

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