36506-46-4

Basic information

• Product Name: 1,2-BIS(4-BROMOPHENOXY)ETHANE
• Synonyms: 1,2-BIS(4-BROMOPHENOXY)ETHANE;1,2-BIS-(P-BROMOPHENOXY)ETHANE
• CAS NO: 36506-46-4
• Molecular Formula: C₁₄H₁₂Br₂O₂
• Molecular Weight: 372.05
• Mol File: 36506-46-4.mol
• Article Data: 8

Chemical Properties

• Melting Point: 134-135 °C
• Boiling Point: 438.7 °C at 760 mmHg
• Flash Point: 182.1 °C
• Appearance: /
• Density: 1.612 g/cm³
• Vapor Pressure: 1.74E-07mmHg at 25°C
• Refractive Index: 1.602
• CAS DataBase Reference: 1,2-BIS(4-BROMOPHENOXY)ETHANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-BIS(4-BROMOPHENOXY)ETHANE(36506-46-4)
• EPA Substance Registry System: 1,2-BIS(4-BROMOPHENOXY)ETHANE(36506-46-4)

Safety Data

• Hazardous Substances Data: 36506-46-4(Hazardous Substances Data)

Usage

Uses

1,2-Bis(4-bromophenoxy)ethane is a useful synthesis intermediate.

InChI:InChI=1/C14H12Br2O2/c15-11-1-5-13(6-2-11)17-9-10-18-14-7-3-12(16)4-8-14/h1-8H,9-10H2

Upstream product

• 106-41-2 4-bromo-phenol 
• 6315-52-2 1,2-bis-tosyloxyethane 
• 106-93-4 ethylene dibromide 
• 104-66-5 1,2-diphenoxyethane 
• 7726-95-6 bromine 
• 64-19-7 acetic acid 
• 100-67-4 potassium phenolate 

Downstream Products

• 1307892-60-9 (Z)-(4,4′-(ethene-1,2-diylbis(oxy))bis(1,4-phenylene))dimethanol 
• 1307892-59-6 (Z)-4,4'-(ethene-1,2-diylbis(oxy))dibenzaldehyde 
• 1044757-88-1 [(η1-Ph2PS-η1)Fe2(CO)6]2(4-μ-SC6H4OCH2CH2OC6H4S-μ-4') 
• 93655-06-2 1,2-Bis-(4-ethinyl-phenoxy)-ethan 
• 255709-12-7 meso-1,2-dibromo-1,2-bis(4-bromophenoxy)-ethane 
• 255709-14-9 trans-1,2-bis(4-bromophenoxy)ethene 
• 255709-15-0 cis-1,2-bis(4-bromophenoxy)ethene 
• 73421-47-3 1,2-cis-diphenoxyethylene 
• 73421-43-9 trans 1,2-dibenzoylethylene 
• 117499-29-3 4-(4-{2-[4-(3-Hydroxy-3-methyl-but-1-ynyl)-phenoxy]-ethoxy}-phenyl)-2-methyl-but-3-yn-2-ol 
• 72659-55-3 C₃₈H₃₂O₂P₂ 

Relevant articles and documents

Therapeutic Nanosystem Consisting of Singlet-Oxygen-Responsive Prodrug and Photosensitizer Excited by Two-Photon Light

Using light as the sole stimulus and employing the generated singlet oxygen as a therapeutic agent and the trigger to activate chemo-drug release could serve as an elegant way to bring into full play the advantageous features of light and enhance therapeu

Design and synthesis of polymeric chiral bicyclo[3.3.0] diene as reusable ligand for rhodium-catalyzed asymmetric 1,4-addition

A series of A-B type sterically regular bicyclio[3.3.0] diene-based polymers were designed and synthesized as immobilized chiral diene ligands for asymmetric catalysis. With polymeric diene 6b, good to excellent enantioselectivities can be achieved in Rh-catalyzed asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated ketones. A series of A-B type sterically regular bicyclio[3.3.0] diene-based polymers were designed and synthesized as immobilized chiral diene ligands for asymmetric catalysis. By using polymeric diene, good to excellent enantioselectivities can be achieved in Rh-catalyzed asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated ketones. Copyright

Synthesis of cis- and trans-1,2-diphenoxyethenes and p,p'-disubstituted diaryloxyethenes

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