54245-33-9

Usage

Uses

Used in Chemical Industries:
3-Bromonaphthalen-2-amine is used as a chemical intermediate for the synthesis of various complex organic compounds. Its unique molecular structure allows it to be a key component in the production of pharmaceuticals, dyes, and other specialty chemicals.
Used in Academic Research:
3-Bromonaphthalen-2-amine is used as a research compound in academic settings to study its chemical properties, reactivity, and potential applications in the development of new materials and compounds. Researchers utilize 3-bromonaphthalen-2-amine to explore its behavior in different reaction conditions and to understand its role in various chemical processes.

InChI:InChI=1/C10H8BrN/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6H,12H2

Upstream product

• 7647-01-0 hydrogenchloride 
• 690244-08-7 1,3-dibromo-2-nitro-naphthalene 
• 84605-00-5 10-bromo-1,2,3,4,5,6,7,8,13,13,14,14-dodecachloro-1,4,4a,4b,5,8,8a,12b-octahydro-11-nitro-1,4-5,8-dimethanotriphenylene 
• 54288-95-8 1,3-dibromonaphthalen-2-amine 
• 64-19-7 acetic acid 
• 67116-33-0 2-bromo-3-nitronaphthalene 
• 107784-15-6 (3-bromo-[2]naphthyl)-carbamic acid ethyl ester 

Downstream Products

• 54245-34-0 3-Brom-2-Naphthonitril 
• 54288-98-1 3-Brom-2-benzylmercaptonaphthalin 
• 16278-49-2 3-Brom-2-benzylsulfonylnaphthalin 
• 59024-98-5 2-(3-Fluoro-naphthalen-2-ylmethyl)-benzoic acid 
• 59024-97-4 2-[1-(3-Fluoro-naphthalen-2-yl)-ethyl]-benzoic acid 
• 59024-96-3 2-(3-Fluor-2-naphthoyl)-benzoesaeure 
• 65776-66-1 N-(3-bromo-[2]naphthyl)-acetamide 
• 54245-35-1 3-Phenacyl-2-naphthoesaeure 
• 54245-36-2 3-Ethoxy-2-naphthoesaeure 
• 25799-29-5 1-[4-(3-Bromo-naphthalen-2-ylsulfanyl)-3-nitro-phenyl]-ethanone 
• 93259-31-5 N-(3-bromo-1-nitro-[2]naphthyl)-toluene-4-sulfonamide 
• 76411-66-0 2-hydrazinonaphtho<2,3-d>thiazole 
• 38824-47-4 2-Phenyl-1H-benzindol 

Relevant academic research and scientific papers

Method of colorimetric analysis of malonic dialdehyde and 4-hydroxy-2-enaldehydes as indexes of lipid peroxidation, kits for carrying out said method, substituted indoles for use in said method and their preparation

A colorimetric assay of enaldehydes or of malonic dialdehyde as lipid peroxidation indices in an aqueous medium including a) addition to the medium of a reagent of a compound of general formula I and their optional addition salts with organic or inorganic bases or with organic or inorganic acids. STR1 in which formula: A and C, which may be identical or different, each represent H, STR2 wherein A and C cannot simultaneously represent H, with: R1 =H; alkyl; aralkyl; aryl substituted on the aryl ring; alkyl sulfonate Y+ ; alkyl phosphonate, Y+ ; or alkyl carboxylate, Y+ ; R2 =H; --OR4 ; F; Cl; Br; I; --NO2 ; SO331 Y+ ; --CN; --COOR4 ; or --CONR5 R6 ; R3 =H; --OR4 ; --NR5 R6 ; --SR4 ; F; Cl; Br; I; --NO2 ; --SO3 --Y+ ; --CN; --COR5 ; --COOR4 ; or --CONR5 R6 ; R4 =H; alkyl; aralkyl; or aryl substituted on the aryl ring; R5 =H; alkyl; aralkyl; or aryl substituted on the aryl ring; R6 =H; aryl, aralkyl; or aryl substituted on the aryl ring; Y+ =cation of an organic or inorganic base; STR3 wherein alkyl represents a linear or branched group comprising 1 to 6 carbon; aryl is substituted on the aryl ring with one or more groups which may be identical or different selected from C1-6 alkyl, alkoxy, hydroxy, amino and carboxyl; b) acidification of the medium; and c) incubation of the acidified medium. Requisites or kits for the implementation of the process are also disclosed.

Relative binding affinity of carboxylate and its isosteres: Nitro, phosphate, phosphonate, sulfonate, and δ-lactone

Using the mono and ditopic receptors 1 and 2 (N-n-butyl-N′-p-tolylurea and 4,8-bis[((n-butylamino)carbonyl)amino]dibenz[b, i]acridan), the relative binding affinities of the title functional groups were determined to be ArOPO32- ≥ ArPO32- > ArCOO- ≥ ArP(OH)O2- > ArOP(OH)O2- > ArSO3- > δ-lactone > ArNO2. No evidence of hydrogen bonding of nitrobenzene to 1 was detected in either CDCl3 or DMSO-d6, but in CCl4, Kassoc = 180 M-1. Ditopic receptor 2 was designed as a receptor for meta-disubstituted aromatic substrates and binds some (isophthalate and 1,3-C6H4(P(OH)O2-)2) with high affinity (Kassoc > 104 M-1) in DMSO-d6. In contrast, the isosteric m-dinitrobenzene is not bound by 2 in that solvent, which further illustrates the relatively poor hydrogen bonding ability of nitro groups.