67973-33-5

Basic information

• Product Name: 3,5-dibroMobenzoic acid ethyl ester
• Synonyms: 3,5-dibroMobenzoic acid ethyl ester;ETHYL 3,5-DIBROMOBENZOATE
• CAS NO: 67973-33-5
• Molecular Formula: C₉H₈Br₂O₂
• Molecular Weight: 307.96662
• Mol File: 67973-33-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 309.2°C at 760 mmHg
• Flash Point: 140.8°C
• Appearance: /
• Density: 1.747g/cm³
• Vapor Pressure: 0.000648mmHg at 25°C
• Refractive Index: 1.572
• CAS DataBase Reference: 3,5-dibroMobenzoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dibroMobenzoic acid ethyl ester(67973-33-5)
• EPA Substance Registry System: 3,5-dibroMobenzoic acid ethyl ester(67973-33-5)

Safety Data

• Hazardous Substances Data: 67973-33-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H8Br2O2/c1-2-13-9(12)6-3-7(10)5-8(11)4-6/h3-5H,2H2,1H3

Upstream product

• 626-39-1 1,3,5-trisbromobenzene 
• 109-94-4 formic acid ethyl ester 
• 58922-06-8 4-amino-3,5-dibromo-benzoic acid ethyl ester 
• 64-17-5 ethanol 
• 1041479-66-6 C₁₂H₆Br₄ClIn 
• 201230-82-2 carbon monoxide 
• 618-58-6 3,5-dibromobenzoic acid 

Downstream Products

• 422569-47-9 3,5-Bis(3-hydroxyprop-1-ynyl)benzoic acid ethyl ester 
• 210355-25-2 3,5-Bis-(3-tert-butoxycarbonylamino-propyl)-benzoic acid ethyl ester 
• 870177-64-3 ethyl 3-bromo-5-{3-{[(benzyloxy)carbonyl]amino}propyl}benzoate 
• 807341-86-2 tert-butyl {3-[3-(3-aminopropyl)-5-(hydroxymethyl)phenyl]propyl}carbamate 
• 807341-84-0 benzyl tert-butyl {[5-(hydroxymethyl)-1,3-phenylene]dipropane-3,1-diyl}bis[carbamate] 
• 807341-90-8 di(tert-butyl) {{5-{{{3-[3-(3-aminopropyl)-5-(hydroxymethyl)phenyl]propyl}amino}carbonyl}-1,3-phenylene}dipropane-3,1-diyl}bis[carbamate] 
• 807341-89-5 di(tert-butyl) {{5-{{{3-{3-{3-{[(benzyloxy)carbonyl]amino}propyl}-5-(hydroxymethyl)phenyl}propyl}amino}carbonyl}-1,3-phenylene}dipropane-3,1-diyl}bis[carbamate] 
• 807341-87-3 dibenzyl {{5-{{{{3-{3-{[(tert-butoxy)carbonyl]amino}propyl}-5-(hydroxymethyl)phenyl}propyl}amino}carbonyl}-1,3-phenylene}dipropane-3,1-diyl}bis[carbamate] 
• 807341-91-9 benzyl tri(tert-butyl) {[5-(hydroxymethyl)-1,3-phenylene]bis(propane-3,1-diyliminocarbonylbenzene-5,1,3-triyldipropane-3,1-diyl)}tetrakis[carbamate] 
• 807341-92-0 tribenzyl tert-butyl {[5-(hydroxymethyl)-1,3-phenylene]bis(propane-3,1-diyliminocarbonylbenzene-5,1,3-triyldipropane-3,1-diyl)}tetrakis[carbamate] 
• 349559-91-7 ethyl 3-{3-{[(benzyloxy)carbonyl]amino}propyl}-5-{3-{[(tert-butoxy)carbonyl]amino}propyl}benzoate 
• 145691-59-4 (3,5-dibromophenyl)methanol 
• 1333113-26-0 C₁₇H₁₈Br₂O 
• 1333113-33-9 C₂₄H₃₁BrO₇ 

Relevant articles and documents

CHEMICAL COMPOUNDS FOR COATING OF NANOSTRUCTURES

The present application relates to a chemical compound comprising an aromatic core, or a carbocyclic, non-aromatic, core, wherein the aromatic core is a benzene ring or a biphenyl; the carbocyclic, non-aromatic core is a 5 to 7 membered ring. The core has

Synthesis of a novel dinuclear ruthenium polypyridine dye for dye-sensitized solar cells application

A new dinuclear ruthenium(II) polypyridine complex has been successfully synthesized. The new compound has been characterized by spectroscopic and electrochemical methods. Its potential application as a sensitizing dye in dye-sensitized solar cells has been checked under AM 1.5 G irradiation conditions (100 mW cm-2) and its performance was compared to that of a commercially available mononuclear analogous dye. The overall light-to-electricity conversion efficiency of the photovoltaic device sensitized by the new dinuclear dye has been found to be over 2.5 times lower than that sensitized by the commercial analogue, despite a much higher extinction coefficient of the former dye. The probable reasons for the lower photovoltaic activity are discussed.

Facile preparation of aromatic esters from aromatic bromides with ethyl formate or DMF and molecular iodine via aryllithium

Various aromatic bromides were treated with n-BuLi and subsequently with ethyl formate, followed by the reaction with ethanol and molecular iodine in the presence of K2CO3 to provide the corresponding aromatic ethyl esters in good yields. Moreover, aromatic bromides could be transformed into the corresponding aromatic methyl esters in good yields by the treatment with n-BuLi and subsequently with DMF, followed by the reaction with methanol, molecular iodine, and K2CO3. Some aromatics could be also converted into the corresponding aromatic esters in good yields by the treatment with n-BuLi, and subsequently with ethyl formate or DMF, followed by the reaction with molecular iodine and K2CO3. The present reactions offer a novel route for the transition-metal-free, carbon-monoxide-free, and therefore environmentally benign one-pot conversion of aromatic bromides and aromatics into aromatic esters.