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Benzamide, N-(4-hydroxyphenyl)-3,5-dinitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99847-35-5

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99847-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99847-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,4 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 99847-35:
(7*9)+(6*9)+(5*8)+(4*4)+(3*7)+(2*3)+(1*5)=205
205 % 10 = 5
So 99847-35-5 is a valid CAS Registry Number.

99847-35-5Relevant academic research and scientific papers

A convenient strategy to functionalize carbon nanotubes with ascorbic acid and its effect on the physical and thermomechanical properties of poly(amide-imide) composites

Mallakpour, Shadpour,Zadehnazari, Amin

, p. 136 - 145 (2014/02/14)

Multi-walled carbon nanotubes (MWCNTs) were functionalized by ascorbic acid by a fast strategy under microwave irradiation to improve interfacial interactions and dispersion of CNTs in a poly(amide-imide) (PAI) matrix. This technique provides a rapid and

Synthesis, antimicrobial, and QSAR studies of substituted benzamides

Kumar, Anil,Narasimhan, Balasubramanian,Kumar, Devinder

, p. 4113 - 4124 (2008/03/11)

A series of new substituted benzamides were synthesized and tested in vitro for their antibacterial activity against Gram-positive and Gram-negative bacteria and as well for antifungal activity. The compounds 8i and 9 showed better activity among the different benzamides synthesized. The structural characteristics governing antibacterial activities of substituted benzamides were studied using QSAR methodology. The results showed that the antimicrobial activity could be modeled using the topological descriptors, molecular connectivity indices (2χv and 2χ) and Kiers shape index (κα1). The low residual activity and high cross-validated r2 values (rcv2) observed indicated the predictive ability of the developed QSAR models.

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