19256-80-5

Usage

Explanation

A chemical compound used in the manufacturing of dyes, pigments, and pharmaceuticals.

Explanation

The base compound from which 1-Hydroxy-3-nitronaphthalene is derived.

Explanation

The molecular composition of 1-Hydroxy-3-nitronaphthalene, indicating the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the compound.

Explanation

The two specific functional groups attached to the naphthalene ring, responsible for the compound's properties and reactivity.

Explanation

The physical appearance of 1-Hydroxy-3-nitronaphthalene, characterized by its yellow color and crystalline structure.

Explanation

The solubility properties of 1-Hydroxy-3-nitronaphthalene, indicating that it does not dissolve in water but dissolves in certain organic solvents.

Explanation

The possible negative health effects of 1-Hydroxy-3-nitronaphthalene, which necessitate proper handling and safety measures.

Derivative

Naphthalene

Functional groups

Hydroxyl and nitro groups

Appearance

Yellow crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Health hazards

Potential irritation to skin, eyes, and respiratory system

Upstream product

• 3229-86-5 3-nitro-1-naphthalenamine 
• 394-93-4 1-Fluoro-3-nitronaphthalin 
• 13802-40-9 1-Methoxy-3-nitronaphthalene 
• 100-39-0 benzyl bromide 
• 13029-24-8 2,4-dinitro-1-naphthalenamine 
• 606-37-1 2,4-dinitronaphthalene 

Downstream Products

• 2764-95-6 4-methoxy-2-naphthylamine 
• 23576-37-6 L-leucine-4-methoxy-2-naphthylamide 
• 104295-15-0 N-benzyloxycarbonyl-L-leucine-(4-methoxy-[2]naphthylamide) 
• 122745-40-8 tert-Butyl(S)-5-(benzyloxy)-1-(chloromethyl)-1,2-dihydro-3H-benzo[e]indole-3-carboxylate 
• 122745-45-3 N-(tert-butyloxycarbonyl)-N-(2-propynyl)-4-(benzyloxy)-1-bromo-2-naphthylamine 
• 122745-38-4 5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-methylidene-1,2-dihydro-3H-benzindole 
• 129918-00-9 5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-methyl-3H-benzindole 
• 122745-37-3 2-((tert-Butyloxycarbonyl)amino)-4-(benzyloxy)-1-bromonaphthalene 
• 122745-36-2 N-(tert-butyloxycarbonyl)-4-(benzyloxy)-2-naphthylamine 
• 122745-35-1 3-Amino-1-(benzyloxy)naphthalene 
• 128228-77-3 5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-(hydroxymethyl)-1,2-dihydro-3H-benzindole, (R)-(-)-O-acetyl mandelate ester 
• 128228-76-2 5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-(hydroxymethyl)-1,2-dihydro-3H-benzindole, (R)-(-)-O-acetylmandelate ester 
• 128300-12-9 5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-(chloromethyl)-1,2-dihydro-3H-benzindole 
• 128300-11-8 5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-(chloromethyl)-1,2-dihydro-3H-benzindole 

Relevant academic research and scientific papers

Improved Synthesis of Several Methoxynitronaphthalenes

An improved procedure for the synthesis of several isomeric methoxynitronaphthalenes is described.The key intermediates in the synthesis are the respective nitronaphthylamines and nitronaphthols.The syntheses of 1-methoxy-3-nitronaphthalene (1), 1-methoxy-5-nitronaphthalene (2), and 2-methoxy-5-nitronaphthalene (3) are reported. Keywords.Methoxynitronaphthalenes; Nitronaphthylamines; Nitronaphthols.

Synthesis of N-(tert-Butyloxycarbonyl)-CBI, CBI, CBI-CDPI1, and CBI-CDPI2: Enhanced Functional Analogues of CC-1065 Incorporating the 1,2,9,9a-Tetrahydrocyclopropabenzindol-4-one (CBI) Left-Hand Subunit

Full details of the synthesis of N-(tert-butyloxycarbonyl)-1,2,9,9a-tetrahydrocyclopropabenzindol-4-one constituting a more stable functional analogue of the CC-1065 left-hand subunit are described.The resolution of an immediate CBI