1309575-94-7

Basic information

• Product Name: (rac)-2-(phenyl)benzo[j]-7-methyl-6-aza-1,3-dioxa-2-boracyclononen-6-ene
• Synonyms: (rac)-2-(phenyl)benzo[j]-7-methyl-6-aza-1,3-dioxa-2-boracyclononen-6-ene
• CAS NO: 1309575-94-7
• Molecular Weight: 265.12
• Mol File: 1309575-94-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (rac)-2-(phenyl)benzo[j]-7-methyl-6-aza-1,3-dioxa-2-boracyclononen-6-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (rac)-2-(phenyl)benzo[j]-7-methyl-6-aza-1,3-dioxa-2-boracyclononen-6-ene(1309575-94-7)
• EPA Substance Registry System: (rac)-2-(phenyl)benzo[j]-7-methyl-6-aza-1,3-dioxa-2-boracyclononen-6-ene(1309575-94-7)

Safety Data

• Hazardous Substances Data: 1309575-94-7(Hazardous Substances Data)

Upstream product

• 1309575-95-8 2,4-diphenylbenzo[j]-9-methyl-8-aza-1,3,5,2,4-trioxadiboracycloundec-8-ene 
• 98-80-6 phenylboronic acid 

Relevant articles and documents

Synthesis, characterization and X-ray studies of new chiral five-six-membered ring, [4.3.0] heterobicyclic system of monomeric boronates

Nine new boronates, six of them chiral, with five-six-membered ring heterobicycles were prepared by reaction of the Schiff bases and phenyl boronic acid. The boronates were fully characterized by spectroscopic techniques, NMR 1H, 13C, 11B, Infrared spectroscopy, mass spectrometry and elemental analysis. The reaction showed high diasteroselectivity, only in the case of compound 4c, containing a methyl substituent in the aliphatic moiety, the induction is low giving a 2:1 mixture of two diatereoisomers. The results showed that the preferred stereochemistry in the heterocycles is that where all substituents in the five membered ring and the phenyl group attached to boron atom are on the same side.