7375-70-4

Basic information

• Product Name: N⁽¹⁾,N⁽²⁾-bis(2-bromobenzyl)-N⁽¹⁾,N⁽²⁾-dimethylpropane-1,3-diamine
• Synonyms: N⁽¹⁾,N⁽²⁾-bis(2-bromobenzyl)-N⁽¹⁾,N⁽²⁾-dimethylpropane-1,3-diamine
• CAS NO: 7375-70-4
• Molecular Weight: 369.099
• Mol File: 7375-70-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N⁽¹⁾,N⁽²⁾-bis(2-bromobenzyl)-N⁽¹⁾,N⁽²⁾-dimethylpropane-1,3-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁽¹⁾,N⁽²⁾-bis(2-bromobenzyl)-N⁽¹⁾,N⁽²⁾-dimethylpropane-1,3-diamine(7375-70-4)
• EPA Substance Registry System: N⁽¹⁾,N⁽²⁾-bis(2-bromobenzyl)-N⁽¹⁾,N⁽²⁾-dimethylpropane-1,3-diamine(7375-70-4)

Safety Data

• Hazardous Substances Data: 7375-70-4(Hazardous Substances Data)

Upstream product

• 698-19-1 N-methyl-2-bromobenzylamine 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 88-65-3 2-bromobenzoic-acid 
• 61436-88-2 2-bromo-N-methylbenzamide 
• 74-89-5 methylamine 
• 7154-66-7 2-bromobenzoic acid chloride 

Downstream Products

• 123268-79-1 Methyl-bis-(2-trimethylsilanyl-benzyl)-amine 
• 1266397-36-7 MeN(CH₂-2-C₆H₄BiPh₂)2 
• 126387-50-6 MeN(CH₂-2-C₆H₄)2BiMe 
• 1266397-38-9 MeN(CH₂-2-C₆H₄BiMe₂)2 
• 35232-96-3 6-Methyl-6,7-dihydro-5H-dibenzazepin 
• 904689-19-6 12-p-fluorophenylethynyl-N-methyl-5,6,7,12-tetrahydrodibenz[c,f][1,5]azastibocine 
• 904689-18-5 12-p-tolylethynyl-N-methyl-5,6,7,12-tetrahydrodibenz[c,f][1,5]azastibocine 
• 126472-97-7 12-phenylethynyl-N-methyl-5,6,7,12-tetrahydrodibenz[c,f][1,5]azastibocine 
• 1195345-85-7 MeN(CH₂-2-C₆H₄SbMe₂)2 

Relevant articles and documents

An amine template strategy to construct successive C-C bonds: Synthesis of benzo[: H] quinolines by a deaminative ring contraction cascade

We developed a convergent strategy to build, cyclize and excise nitrogen from tertiary amines for the synthesis of polyheterocyclic aromatics. Biaryl-linked azepine intermediates can undergo a deaminative ring contraction cascade reaction, excising nitrogen with the formation of an aromatic core. This strategy and deaminative ring contraction reaction are useful for the synthesis of benzo[h]quinolines. This journal is

TRANSANNULAR BOND FORMATION BETWEEN THE ANTIMONY AND THE NITROGEN ATOMS IN DIBENZAZASTIBOCINE SYSTEM. FORMATION OF X-Sb-X AND X-Sb-N(1+) HYPERVALENT BOND

6-Methyl-5,6,7,12-tetrahydro-12-p-tolyldibenzazastibocine (1) was prepared by means of one-pot reaction of di(o-bromobenzyl)methylamine (2), butyllithium, and antimony trichloride, followed by p-tolyllithium in 23percent yield.Halogenation of 1