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Benzonitrile, 4,4'-[1,9-nonanediylbis(oxy)]bis-, also known as Bis(4-cyanophenyl) nonane, is an organic compound with the chemical formula C21H27N2O2. It is a colorless to pale yellow liquid with a molecular weight of 341.45 g/mol. Benzonitrile, 4,4'-[1,9-nonanediylbis(oxy)]bis- is characterized by its two benzonitrile groups connected by a nonane linker, which consists of a 1,9-nonanediyl bis(oxy) chain. It is primarily used as a monomer in the synthesis of various polymers, particularly in the production of polyamides and polyimides, due to its ability to form strong, heat-resistant materials. The compound is also known for its potential applications in the pharmaceutical and chemical industries, where it may be used as an intermediate in the synthesis of complex molecules.

1248-95-9

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1248-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1248-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,4 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1248-95:
(6*1)+(5*2)+(4*4)+(3*8)+(2*9)+(1*5)=79
79 % 10 = 9
So 1248-95-9 is a valid CAS Registry Number.

1248-95-9Relevant academic research and scientific papers

Structure-Activity Studies with Bis-Amidines That Potentiate Gram-Positive Specific Antibiotics against Gram-Negative Pathogens

Wesseling, Charlotte M. J.,Slingerland, Cornelis J.,Veraar, Shanice,Lok, Samantha,Martin, Nathaniel I.

, p. 3314 - 3335 (2021/11/24)

Pentamidine, an FDA-approved antiparasitic drug, was recently identified as an outer membrane disrupting synergist that potentiates erythromycin, rifampicin, and novobiocin against Gram-negative bacteria. The same study also described a preliminary structure-activity relationship using commercially available pentamidine analogues. We here report the design, synthesis, and evaluation of a broader panel of bis-amidines inspired by pentamidine. The present study both validates the previously observed synergistic activity reported for pentamidine, while further assessing the capacity for structurally similar bis-amidines to also potentiate Gram-positive specific antibiotics against Gram-negative pathogens. Among the bis-amidines prepared, a number of them were found to exhibit synergistic activity greater than pentamidine. These synergists were shown to effectively potentiate the activity of Gram-positive specific antibiotics against multiple Gram-negative pathogens such as Acinetobacter baumannii, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Escherichia coli, including polymyxin- and carbapenem-resistant strains.

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