107046-99-1

Basic information

• Product Name: (6,8,10-trinitro-1,4-dioxaspiro<4,5>deca-6,9-dienato)sodium
• Synonyms: (6,8,10-trinitro-1,4-dioxaspiro<4,5>deca-6,9-dienato)sodium
• CAS NO: 107046-99-1
• Molecular Weight: 295.141
• Mol File: 107046-99-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (6,8,10-trinitro-1,4-dioxaspiro<4,5>deca-6,9-dienato)sodium(CAS DataBase Reference)
• NIST Chemistry Reference: (6,8,10-trinitro-1,4-dioxaspiro<4,5>deca-6,9-dienato)sodium(107046-99-1)
• EPA Substance Registry System: (6,8,10-trinitro-1,4-dioxaspiro<4,5>deca-6,9-dienato)sodium(107046-99-1)

Safety Data

• Hazardous Substances Data: 107046-99-1(Hazardous Substances Data)

Upstream product

• 7388-28-5 sodium 2-hydroxyethoxide 
• 606-35-9 1-methoxy-2,4,6-trinitrobenzene 
• 4732-14-3 2,4,6-trinitro-phenetole 

Downstream Products

• 3324-58-1 sodium picrate 
• 6478-31-5 1-(2-hydroxyethoxy)-2,4,6-trinitrobenzene 

Relevant articles and documents

REACTIONS OF AROMATIC NITRO COMPOUNDS. LXIV. ANIONIC ? COMPLEXES OF THE ALKYL ETHERS OF 2,4,6-TRINITROPHENOL WITH THE ALCOHOLATES OF DIHYDRIC AND TRIHYDRIC ALCOHOLS

Sodium 1-methoxy-1-(β-hydroxypropoxy)-2,4,6-trinitro-2,5-cyclohexadienide was obtained from 2,4,6-trinitroanisole and sodium 2-hydroxypropoxide.It was then converted into corresponding spirocyclic anionic ? complex.In the reaction of 2,4,6-trinitrophenetole with sodium 2-hydroxyethoxide, 3-hydroxypropoxide, and 4-hydroxybutoxide the 1-ethoxy-1-hydroxyalkoxyl ? complexes are formed at the first stage and are then converted into spirocyclic and 1,1-dihydroxyalkoxyl ? complexes.Spirocyclization only takes place in the presence of the β-hydroxy group.The transformations are realized with the participation of the glycol ethers of 2,4,6-trinitrophenol, which are formed in the reaction as transetherification products.