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Dimethyl-[3-(3-methyl-4-nitro-phenoxy)-propyl]-amine is a complex organic compound with the molecular formula C12H18N2O3. It features a central nitrogen atom bonded to two methyl groups and a propyl chain, which is further connected to a 3-methyl-4-nitro-phenoxy group. This phenoxy group consists of a benzene ring with a methyl group at the third position and a nitro group at the fourth position, attached to the propyl chain through an oxygen atom. The compound's structure and properties make it a potential candidate for various chemical and pharmaceutical applications, such as a precursor in the synthesis of pharmaceuticals or as an intermediate in the production of agrochemicals. Its specific reactivity and stability are influenced by the presence of the nitro group, which can participate in various chemical reactions, and the overall molecular structure.

2287-13-0

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2287-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2287-13-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2287-13:
(6*2)+(5*2)+(4*8)+(3*7)+(2*1)+(1*3)=80
80 % 10 = 0
So 2287-13-0 is a valid CAS Registry Number.

2287-13-0Relevant academic research and scientific papers

Benzophenone Derivatives: A Novel Series of Potent and Selective Inhibitors of Human Immunodeficiency Virus Type 1 Reverse Transcriptase

Wyatt, Paul G.,Bethell, Richard C.,Cammack, Nicholas,Charon, Daniel,Dodic, Nerina,et al.

, p. 1657 - 1665 (2007/10/02)

A series of benzophenone derivatives has been synthesized and evaluated as inhibitors of HIV-1 reverse transcriptase (RT) and the growth of HIV-1 in MT-4 cells.Through the use of the structure-activity relationships within this series of compounds and computational chemistry techniques, a binding conformation is proposed.The SAR also indicated that the major interactions of 1h with the RT enzyme are through hydrogen bonding of the amide and benzophenone carbonyls and ?-orbital interactions with the benzophenone nucleus and an aromatic function separated from the benzophenone by a suitable spacer group.The crystal structure of compound 1h has been determined.A number of compounds with potent inhibitory activity against HIV-1 RT and HIV in cellular assays at levels comparable with AZT and our efforts to identify a metabolically stable analogue are described.

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