92670-09-2

Basic information

• Product Name: Benzene, 1,5-dibromo-2,3,4-trimethoxy-
• CAS NO: 92670-09-2
• Molecular Formula: C9H10Br2O3
• Molecular Weight: 325.985
• Mol File: 92670-09-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1,5-dibromo-2,3,4-trimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,5-dibromo-2,3,4-trimethoxy-(92670-09-2)
• EPA Substance Registry System: Benzene, 1,5-dibromo-2,3,4-trimethoxy-(92670-09-2)

Safety Data

• Hazardous Substances Data: 92670-09-2(Hazardous Substances Data)

Upstream product

• 56-23-5 tetrachloromethane 
• 634-36-6 1,2,3-trimethoxybenzene 
• 7726-95-6 bromine 
• 10385-36-1 2,3,4-trimethoxybromobenzene 
• 91-10-1 1,3-dimethoxy-2-hydroxy-benzene 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 860692-88-2 5-allyl-2,3,4-trimethoxybenzoic acid 
• 1314438-97-5 C₅₁H₃₈N₆O₃ 
• 17345-74-3 4,5,6-tribromo-pyrogallol 
• 318235-07-3 2-eneEbelacol C 
• 99512-65-9 1,3-dibromo-4,5,6-trimethoxy-2-nitro-benzene 
• 92669-97-1 1,5-bis(trimethylsilyl)-2,3,4-trimethoxybenzene 

Relevant articles and documents

Probing a hidden world of molecular self-assembly: Concentration-dependent, three-dimensional supramolecular interconversions

A terpyridine-based, concentration-dependent, facile self-assembly process is reported, resulting in two three-dimensional metallosupramolecular architectures, a bis-rhombus and a tetrahedron, which are formed using a two-dimensional, planar, tris-terpyri

Facile catch and release of fullerenes using a photoresponsive molecular tube

A novel M2L2 molecular tube capable of binding fullerene C60 was synthesized from bispyridine ligands with embedded anthracene panels and Ag(I) hinges. Unlike previous molecular cages and capsules, this open-ended tubular host can accommodate a single molecule of various C60 derivatives with large substituents. The fullerene guest can then be released by using the ideal, noninvasive external stimulus, light.

Practical and regioselective brominations of aromatic compounds using tetrabutylammonium peroxydisulfate

Direct bromination of wide range of aromatic compounds substituted with electron donating groups such as methoxy, hydroxy, or amino groups have been achieved with high regioselectivity by the reaction with Br2 in the presence of tetrabutylammonium peroxydisulfate 1 under mild conditions in acetonitrile in excellent yields. The use of lithium bromide as a bromination reagent afforded high yields of monobromo compounds with complete regioselectivity under neutral and mild reaction conditions in acetonitrile.