5273-61-0

Basic information

• Product Name: 5,6-dibromocyclohex-2-ene-1,4-dione
• Synonyms: 5,6-dibromocyclohex-2-ene-1,4-dione
• CAS NO: 5273-61-0
• Molecular Formula: C₆H₄Br₂O₂
• Molecular Weight: 267.92
• Mol File: 5273-61-0.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 312.2°Cat760mmHg
• Flash Point: 131.5°C
• Appearance: /
• Density: 2.205g/cm³
• Vapor Pressure: 0.000535mmHg at 25°C
• Refractive Index: 1.628
• CAS DataBase Reference: 5,6-dibromocyclohex-2-ene-1,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 5,6-dibromocyclohex-2-ene-1,4-dione(5273-61-0)
• EPA Substance Registry System: 5,6-dibromocyclohex-2-ene-1,4-dione(5273-61-0)

Safety Data

• Hazardous Substances Data: 5273-61-0(Hazardous Substances Data)

Usage

General Description

5,6-dibromocyclohex-2-ene-1,4-dione is a chemical compound with the molecular formula C6H4Br2O2. It is a yellow solid at room temperature and is primarily used in organic synthesis and as a building block for various chemical reactions. 5,6-dibromocyclohex-2-ene-1,4-dione is an important intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals. It is also used as a reagent in the preparation of other organic compounds. Additionally, 5,6-dibromocyclohex-2-ene-1,4-dione is known for its strong oxidizing properties and can react with a wide range of organic compounds, making it a versatile and valuable chemical in the field of organic chemistry.

InChI:InChI=1/C6H4Br2O2/c7-5-3(9)1-2-4(10)6(5)8/h1-2,5-6H

Upstream product

• 7726-95-6 bromine 
• 106-51-4 p-benzoquinone 
• 69945-44-4 (1RS,2SR,3RS,4RS)-2,3-dibromocyclohex-5-ene-1,4-diol 
• 169529-93-5 (-)-2,3-dibromocyclohex-5-ene-1,4-diol 

Downstream Products

• 105143-22-4 2,5-bis-[(2-hydroxy-ethyl)-methyl-amino]-[1,4]benzoquinone 
• 123-31-9 hydroquinone 
• 10035-10-6 hydrogen bromide 
• 6363-31-1 2,4-dibromo-1,4-dihydroxybenzene 
• 18376-35-7 (1α,2β,3α,4β,5β,6β)-1,2-dibromo-3,4,5,6-tetraacetoxycyclo-hexane 
• 18376-35-7 (1α,2β,3α,4α,5β,6β)-1,2-dibromo-3,4,5,6-tetraacetoxycyclohexane 
• 145047-67-2 Acetic acid (1R,2S,3S,4R,5S,6R)-4-acetoxy-2,3-dibromo-5,6-dihydroxy-cyclohexyl ester 
• 18376-36-8 (1S,2S,3S,4S,5R,6R)-5,6-Dibromo-cyclohexane-1,2,3,4-tetraol 
• 4381-96-8 (+/-)-tetraacetylconduritol C 
• 4381-96-8 (+/-)-1,2,3,4-tetra-O-acetylconduritol E 
• 526-87-4 (+/-)-conduritol C 
• 526-87-4 conduritol-E 
• 39078-08-5 rac-(3R,4R,5R,6R)-3,4:5,6-diepoxycyclohex-1-ene 
• 120494-27-1 (1RS,2RS,3RS,6RS)-3,6-di(phenylthio)cyclohex-4-ene-1,2-diol 

Relevant articles and documents

Concise syntheses and some biological activities of dl-2,5-di-O-methyl-chiro-inositol, dl-1,4-di-O-methyl-scyllo-inositol, and dl-1,6-dibromo-1,6-dideoxy-2,5-di-O-methyl-chiro-inositol

The regio- and stereospecific synthesis of O-methyl-chiro-inositols and O-methyl-scyllo-inositol was achieved, starting from p-benzoquinone. After preparing dimethoxy conduritol-B as a key compound, regiospecific bromination of the alkene moiety of dimeth

LADDERANE LIPID COMPOUNDS AND LIPOSOMES AND METHODS OF PREPARING AND USING THE SAME

Methods for preparing a variety of ladderane precursors, ladderane compounds and ladderane lipids are provided. Also provided are methods of preparing a liposome from the ladderane lipids disclosed herein, and compositions thereof. Aspects of the invention include encapsulated one or more cargo moieties in the liposome or compositions thereof and use of the subject liposome compositions as vehicles in drug delivery, imaging, diagnostics and other medical applications. Aspects of the methods disclosed herein include administering a liposomal composition comprising a pharmaceutical agent to a subject under conditions sufficient to deliver the composition to a site of interest in the subject, and release the pharmaceutical agent from the liposomal composition.

Synthesis of novel mono and bis-indole conduritol derivatives and their α/β-glycosidase inhibitory effects

Here we synthesized four novel indole conduritol derivatives 1-4 for the first time in the literature and probed their biological activities with the α and β-glucosidases. The compounds showed quite effective glucosidase inhibitory action. IC50