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943967-10-0

2',1,3,2'''-tetra-N-benzyloxycarbonylparomomycin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 943967-10-0 Structure

  • Basic information

    1. Product Name: 2',1,3,2'''-tetra-N-benzyloxycarbonylparomomycin
    2. Synonyms: 2',1,3,2'''-tetra-N-benzyloxycarbonylparomomycin
    3. CAS NO:943967-10-0
    4. Molecular Formula:
    5. Molecular Weight: 1152.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 943967-10-0.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: 2',1,3,2'''-tetra-N-benzyloxycarbonylparomomycin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2',1,3,2'''-tetra-N-benzyloxycarbonylparomomycin(943967-10-0)
    11. EPA Substance Registry System: 2',1,3,2'''-tetra-N-benzyloxycarbonylparomomycin(943967-10-0)

  • 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: 943967-10-0(Hazardous Substances Data)

943967-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943967-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,9,6 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 943967-10:
(8*9)+(7*4)+(6*3)+(5*9)+(4*6)+(3*7)+(2*1)+(1*0)=210
210 % 10 = 0
So 943967-10-0 is a valid CAS Registry Number.

943967-10-0Upstream product

943967-10-0Downstream Products

943967-10-0Relevant articles and documents

Robust polymeric nanoparticles for the delivery of aminoglycoside antibiotics using carboxymethyldextran-b-poly(ethyleneglycols) lightly grafted with n-dodecyl groups

Soliman, Ghareb M.,Szychowski, Janek,Hanessian, Stephen,Winnik, Franoise M.

, p. 4504 - 4514 (2010)

Aminoglycoside antibiotics are effective in the treatment of infections caused by aerobic Gram negative bacilli, but their widespread use is hampered by serious side effects that may be alleviated through the use of tailored delivery systems. Robust polyi

6-Hydroxy to 6?-amino tethered ring-to-ring macrocyclic aminoglycosides as probes for APH(3′)-IIIa kinase

Hanessian, Stephen,Szychowski, Janek,Campos-Reales Pineda, Natalhie B.,Furtos, Alexandra,Keillor, Jeffrey W.

, p. 3221 - 3225 (2008/02/03)

Based on molecular modeling and available X-ray structure data on aminoglycosides complexed with a bacterial ribosomal surrogate or with a kinase, two analogues of paromomycin were prepared by tethering the 6-OH and the 6?-NH2 group with a five

Novel conjugates of polysaccharides and uses thereof

-

Page/Page column 16-17; 1/3, (2008/06/13)

Novel conjugates composed of a saccharide-containing moiety (e.g., aminoglycosides) covalently linked to a moiety containing two or more basic amino acid residues (e.g., a polyarginine) and processes of preparing same are disclosed. Further disclosed are

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