119450-03-2

Usage

Chemical Properties

Yellow Powder

InChI:InChI=1/C9H7Br3O2/c10-6-4-2-1-3-5(6)7(11)8(12)9(13)14/h1-4,7-8H,(H,13,14)

Upstream product

• 7345-79-1 2-bromocinnamic acid 
• 67-66-3 chloroform 
• 7726-95-6 bromine 
• 121263-08-9 (2-bromo-benzylidene)-malonic acid 
• 6630-33-7 ortho-bromobenzaldehyde 
• 7345-79-1 2-bromocinnamic acid 

Downstream Products

• 153140-75-1 1-bromo-2-[(Z)-2-bromoethenyl]benzene 
• 137072-83-4 1-phenyl-1-benzophosphepine 
• 154467-43-3 (Z)-1-(o-bromophenyl)-4-trimethylsilyl-1-buten-3-yne 
• 154467-45-5 5-Phenyl-6-trimethylsilanyl-5H-5-phospha-benzocycloheptene 
• 154467-46-6 5-Phenyl-6-trimethylsilanyl-5H-5-arsa-benzocycloheptene 
• 154081-41-1 1-phenyl-1-benzoarsepine 
• 154467-44-4 (Z,Z)-1-bromo-4-(2-bromophenyl)-1-trimethylsilyl-1,3-butadiene 
• 246876-11-9 1-phenyl-2-trimethylsilyl-1-benzophosphepine 1-oxide 

Relevant academic research and scientific papers

Carbene-catalyzed LUMO activation of alkyne esters for access to functional pyridines

A carbene-catalyzed LUMO activation of α,β-unsaturated alkyne esters is reported. This catalytic process allows for effective reactions of alkyne esters with enamides to synthesize functional pyridines via simple protocols. A previously unexplored unsaturated alkyne acyl azolium intermediate is involved in the key step of the reaction.

A versatile synthesis of 1-benzoheteroepines containing group 14, 15, and 16 heavier elements via a common 1,6-dilithium intermediate

Fully unsaturated group 14 (Si, Ge, and Sn), group 15 (P, As, Sb, and Bi) and group 16 (S, Se, and Te) 2-trimethylsilyl-1-benzoheteroepines (16a- j), including the first isolated examples of bismepines, have been prepared by reaction of the corresponding electrophilic metal reagents (MX2 or MX4; M=group 14, 15, and 16 heavier elements) with the key 1,6-dilithium intermediate (9), generated from the common starting compound (Z,Z)-1-bromo- 4-(2-bromophenyl)-1-trimethylsilyl-1,3-butadiene (14) by treatment with tert- butyllithium. The trimethylsilyl group in 16b-j was readily removed by treatment with tetrabutylammonium fluoride to give the desired C- unsubstituted 1-benzoheteroepines (1b-j). Single crystal X-ray analyses of 1d (P) and 1f (Sb) revealed that the seven-membered rings exist in boat conformations with the heteroatoms at the bows. All obtained C-unsubstituted group 15 and 16 1-benzoheteroepines (1d-j) were thermolabile in solution towards heteroatom extrusion, while heteroepines (16d-j) having the bulky trimethylsilyl group at the 2-position were much more stable than 1d-j. The half-lives of 1d-j estimated from 1H-NMR spectral analysis indicate that the thermal stabilities of 1d-j decrease in the order 1f (Sb)>1d (P)>1e (As)>1g (Bi) in the group 15 heteroepines and 1j (Te)>1i (Se)>1h (S) in the group 16 heteroepines.