35704-34-8

Basic information

• Product Name: 2,4-Dichloro-1,2,3,4-tetrahydro-3-(1-naphthalenyl)naphtho[2,1-e]-1,3,2,4-diazadiborine
• Synonyms: 2,4-Dichloro-1,2,3,4-tetrahydro-3-(1-naphthalenyl)naphtho[2,1-e]-1,3,2,4-diazadiborine
• CAS NO: 35704-34-8
• Molecular Formula: C₂₀H₁₄B₂Cl₂N₂
• Molecular Weight: 374.86656
• Mol File: 35704-34-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4-Dichloro-1,2,3,4-tetrahydro-3-(1-naphthalenyl)naphtho[2,1-e]-1,3,2,4-diazadiborine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Dichloro-1,2,3,4-tetrahydro-3-(1-naphthalenyl)naphtho[2,1-e]-1,3,2,4-diazadiborine(35704-34-8)
• EPA Substance Registry System: 2,4-Dichloro-1,2,3,4-tetrahydro-3-(1-naphthalenyl)naphtho[2,1-e]-1,3,2,4-diazadiborine(35704-34-8)

Safety Data

• Hazardous Substances Data: 35704-34-8(Hazardous Substances Data)

Upstream product

• 134-32-7 1-amino-naphthalene 
• 10294-34-5 boron trichloride 
• 13524-20-4 α naphthylamine trichloroborane 

Downstream Products

• 11113-50-1 boric acid 
• 552-46-5 1-naphthylamine hydrochloride 

Relevant articles and documents

HETEROCYCLES RELATED TO 2,4-DIBORA 1,3-DIAZAROBENZENE

The reaction of ortho-substituted arylamines oY-C6H4NH2 (Y=H, Cl, Br, Me) with BX3, (X=F, Cl, Br, I) was investigated.By suitable choice of Y and X, this reaction may be directed to obtain, in a quantitative way, a new kind of heterocycle I instead of the expected trimeric species (oYC6H4NBX)3.The formation of I was found to be related to the bulk of Y substituent and to the nature of X, increasing in the order BCl3 a tertiary amine added, always gives the corresponding borazines.Some derivatives of I were prepared (X=Me, Y=Br, Me) and characterized by NMR (1H, 13C and 11B) and mass spectra. In connection with this study, we were led to the question of atropisomerism in the N-triarylborazines (oYC6H4NBX)3 when the starting arylamine bears an ortho substituent Y.As far as the compound Y=Me, X=Me is concerned, a sole isomer, the C3t one, could be obtained instead of the two expected.