4793-98-0

Usage

Chemical Compound

Yes

Usage

Explosive
Rocket propellant

Physical State

Yellow crystalline solid

Sensitivity

Highly sensitive to shock and friction

Power

Powerful explosive

Stability

High

Melting Point

Low

Applications

Military applications
Manufacturing of ammunition
Fireworks

Health Risks

Highly toxic and carcinogenic

Environmental Risks

Significant

Safety Precautions

Must be handled with extreme caution and in accordance with strict safety protocols.

Upstream product

• 2243-95-0 1,4,5-trinitronaphthalene 
• 605-71-0 1,5-dinitronaphthalene 
• 86-57-7 1-Nitronaphthalene 

Downstream Products

• 3432-57-3 1,4,5,8-tetrachloronaphthalene 
• 475-38-7 5,8-Dihydroxy-1,4-naphthoquinone 
• 2187-88-4 1,4,5,8-tetra(amino)naphthalene 
• 2243-62-1 1,5-naphthalenediamine 
• 10075-69-1 N₁,N₁,N₅,N₅-tetramethyl-1,5-diaminonaphthalene 

Relevant academic research and scientific papers

A 1, 4, 5, 8-tetrahydro-naphthalene tin chloride hydrochloride method for the preparation of

The invention discloses a method for preparing 1,4,5,8-tetraaminonaphthalene tin chloride hydrochloride and relates to a method for preparing hydrochloride. The method aims at solving the technical problems of more by-products, high cost, low yield, tedious after-treatment and difficulty in industrial large-scale production of the existing method for preparing 1,4,5,8-tetraaminonaphthalene tin chloride hydrochloride. The method disclosed by the invention comprises the following steps: firstly, preparing high-purity 1,4,5,8-tetranitronaphthalene; and secondly, preparing high-purity 1,4,5,8-tetraaminonaphthalene tin chloride hydrochloride. Due to the method, high-purity 1,4,5,8-tetranitronaphthalene which is difficult to synthesize by virtue of the conventional method can be successfully prepared and 1,4,5,8-tetraaminonaphthalene tin chloride hydrochloride is prepared from stannous chloride and concentrated hydrochloric acid in high efficiency by virtue of adding catalytic addictives and the operation process is simplified. The method has the advantages of inexpensive and available selected raw materials, high yield, low cost and environmental friendliness and is suitable for industrial scale-up. The method is applied in the field of preparation of organic intermediate.

TETRAAMINE DERIVATIVE, METHOD FOR PRODUCING THE SAME, AND ORGANIC ELECTRONIC DEVICE USING THE SAME

PROBLEM TO BE SOLVED: To provide a tetraamine derivative having naphthalene or perylene as a skeleton with cyclic urea bonds, which can be used as a coating-type organic semiconductor material such as an organic thin film transistor (organic TFT), an organic electroluminescent element (organic EL element), and an organic thin film solar cell, and a method for synthesizing the same. SOLUTION: There is provided as a coating-type semiconductor material, for example, a tetraamine derivative having a naphthalene skeleton with cyclic urea bonds, which can be obtained according to the following reaction formula. COPYRIGHT: (C)2015,JPOandINPIT