954-46-1

Usage

Uses

Used in Pharmaceutical Synthesis:
9-Nitrophenanthrene is utilized as a precursor in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a key intermediate in the production of drugs that target specific medical conditions.
Used in Organic Compound Synthesis:
Beyond its pharmaceutical applications, 9-Nitrophenanthrene is also employed in the synthesis of other organic compounds. Its versatility in chemical reactions makes it a valuable component in the creation of a wide range of organic molecules.
Used in Environmental Research:
9-Nitrophenanthrene serves as a research tool in the study of environmental pollutants. It helps scientists understand the impact of such pollutants on human health and the environment, contributing to the development of strategies for pollution control and prevention.
Used in Chemical Education and Analysis:
In academic and research settings, 9-Nitrophenanthrene is used for educational purposes and in analytical chemistry. It provides a practical example of a nitro derivative and can be employed in experiments that explore the properties and reactions of polycyclic aromatic hydrocarbons.
While the provided materials do not specify different industries for the uses of 9-Nitrophenanthrene, the applications listed above can be relevant across various sectors such as pharmaceuticals, environmental science, chemical research, and education.

InChI:InChI=1/C14H9NO2/c16-15(17)14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9H

Upstream product

• 85-01-8 phenanthrene 
• 7697-37-2 nitric acid 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 68572-87-2 9-phenanthrenylboronic acid 

Downstream Products

• 947-73-9 9-Aminophenanthrene 
• 215-64-5 dibenzo[a,c]phenacine 
• 165329-56-6 2H-Dibenzo[e,g]isoindole-1-carboxylic acid benzyl ester 
• 14140-04-6 phenanthrene-9,10-dione oxime 
• 4235-09-0 9-(N-acetylamino)phenanthrene 
• 302595-31-9 benzylidene-[9]phenanthryl-amine 
• 81593-08-0 N-9-phenanthrenylbenzamide 
• 883-20-5 9-methylphenanthrene 
• 17181-05-4 (E)-9-styrylphenanthrene 
• 17181-04-3 cis-1-phenyl-2-(9-phenanthryl)ethene 
• 7509-44-6 10-diazophenanthren-9(10H)-one 
• 235-93-8 phenanthro<9,10-c>pyrrole 

Relevant academic research and scientific papers

Ipso-nitration of arylboronic acids with bismuth nitrate and perdisulfate

An efficient and one pot synthetic method of ipso-nitration of arylboronic acids has been developed. The high efficiency, general applicability, and broader substrate scope including heterocycles and functional groups make this method advantageous. Due to its simplicity, we expect to find application of this method in synthesis.

Reactions of gas-phase phenanthrene under simulated atmospheric conditions

Rate constants for the gas-phase reactions of phenanthrene with OH radicals, NO3 radicals, and O3 have been determined at 296 ± 2 K and atmospheric pressure of air. The rate constants obtained (in cm3 molecule- 1 s-1 units) were (1.27 ± 0.23) x 10-11 for the OH radical reaction, (1.2 ± 0.4) x 10-13 for the NO3 radical reaction under atmospheric conditions, and (4.0 ± 1.0) x 10-19 for the O3 reaction. These rate constants indicate that the OH radical and NO3 radical reactions will be the dominant atmospheric loss processes for phenanthrene and that the overall atmospheric lifetime of gas-phase phenanthrene will be ≤1 day. Mutagenicity bioassays and chemical analyses of the products of the NO3 radical reaction and NO(x)-air photooxidation of phenanthrene were also conducted.

The Formation of Monomeric and Dimeric Nitro Nitrates in the Reaction of Phenanthrene with Nitrogen Dioxide; X-Ray Crystal Structure of trans-10-Nitro-9,10-dihydrophenanthren-9-yl Nitrate

Reaction of phenanthrene (1) with nitrogen dioxide in benzene solution gives the dimeric nitro nitrate (3), trans and cis nitro nitrates (7) and (8), and 9-nitro- (4), 3-nitro- (5) and 1-nitro-pnenanthrene (6).The X-ray crystal structure of the trans nitro nitrate (7) is reported.The effect of the phenanthrene (1) concentration on product yields is reported.Gas-liquid chromatography results for the nitro nitrates (3) and (7) point to difficulties in using this technique for product analyses in reactions of phenanthrene (1) with nitrogen dioxide.

Reactions of Phenanthrenes with Nitrogendioxid in UV Light

The compounds 2-7 were isolated from solutions of phenanthrene (1) and nitrogendioxide in carbon tetrachloride after irradiation with UV light having long wavelengths (λ > 290 nm).With the help of spectroscopical methods the proposed structures are derived.Radical mechanisms are proposed for these reactions. - Key words: Phenanthrene, Nitrogendioxid, UV Light