Recommended Products
Quality Level
Assay
97%
form
solid
mp
70-75 °C (lit.)
SMILES string
CC(=O)Oc1ccc(OC(C)=O)c(Br)c1
InChI
1S/C10H9BrO4/c1-6(12)14-8-3-4-10(9(11)5-8)15-7(2)13/h3-5H,1-2H3
InChI key
XRIFNWOHWJOCQG-UHFFFAOYSA-N
General description
1,4-Diacetoxy-2-bromobenzene can be prepared by reacting 1,4-benzoquinone with zinc bromide in the presence of acetic anhydride.
Application
1,4-Diacetoxy-2-bromobenzene may be used to synthesize bromohydroquinone and (Sp,S)-1-(2,5-diacetoxyphenyl)-2-(p-tolylsulfinyl)ferrocene.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Highly Selective Negishi Cross-Coupling Reaction of a Zinc-Metallated Ferrocenyl p-Tolyl Sulfoxide: New Chiral Ferrocene-Based Quinone Ligands.
European Journal of Organic Chemistry, 15, 2756-2763 (2003)
Design, Synthesis, and Evaluation of Synthetic Mimics of Cell Surface Receptors, 212-212 (2007)
Total synthesis of siccayne.
Synthesis, 10, 935-937 (1990)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service