589-87-7,MFCD00001051
Catalog No.:AA0032N4

589-87-7 | 1-Bromo-4-iodobenzene

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
99%
in stock  
$10.00   $7.00
- +
25g
99%
in stock  
$15.00   $10.00
- +
100g
99%
in stock  
$38.00   $26.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0032N4
Chemical Name:
1-Bromo-4-iodobenzene
CAS Number:
589-87-7
Molecular Formula:
C6H4BrI
Molecular Weight:
282.9044
MDL Number:
MFCD00001051
SMILES:
Brc1ccc(cc1)I
NSC Number:
8033
Properties
Properties
 
BP:
252.0°C  
Form:
Solid  
MP:
89-91 °C(lit.);  
Refractive Index:
1.6618 (estimate)  
Solubility:
0.008g/l  
Stability:
Light Sensitive  
Storage:
Light sensitive;Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
66.9  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
0  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4  

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.PerkintransactionsI,1983,p.2077-2087

[1]ChemistryLetters,1983,p.1201-1202

[1]JournaloftheAmericanChemicalSociety,1982,vol.104,p.3917-3923

[1]JournaloftheAmericanChemicalSociety,1977,vol.99,p.5249-5253

[1]AngewandteChemie-InternationalEdition,1998,vol.37,p.1701-1703

Literature

Title: Copper-catalyzed one-pot multicomponent coupling reaction of phenols, amides, and 4-bromphenyl iodide.

Journal: Organic letters 20081016

Title: Orientational isomerism and binding ability of nonsymmetrical guests encapsulated in a self-assembling heterodimeric capsule.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20050805

Title: Synthesis of N tau-arylhistidine derivatives via direct N-arylation.

Journal: Bioorganic & medicinal chemistry letters 20040405

Quotation Request
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Additional Info:
SDS
Tags:589-87-7 Molecular Formula|589-87-7 MDL|589-87-7 SMILES|589-87-7 1-Bromo-4-iodobenzene
Catalog No.: AA0032N4
589-87-7,MFCD00001051
589-87-7 | 1-Bromo-4-iodobenzene
Pack Size: 10g
Purity: 99%
in stock
$10.00 $7.00
Pack Size: 25g
Purity: 99%
in stock
$15.00 $10.00
Pack Size: 100g
Purity: 99%
in stock
$38.00 $26.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA0032N4
Chemical Name: 1-Bromo-4-iodobenzene
CAS Number: 589-87-7
Molecular Formula: C6H4BrI
Molecular Weight: 282.9044
MDL Number: MFCD00001051
SMILES: Brc1ccc(cc1)I
NSC Number: 8033
Properties
BP: 252.0°C  
Form: Solid  
MP: 89-91 °C(lit.);  
Refractive Index: 1.6618 (estimate)  
Solubility: 0.008g/l  
Stability: Light Sensitive  
Storage: Light sensitive;Keep in dry area;Room Temperature;  
Complexity: 66.9  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 0  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4  
Downstream Synthesis Route
525-76-8    589-87-7    1140-17-6 

[1]JournaloftheChemicalSociety.PerkintransactionsI,1983,p.2077-2087

201230-82-2    65826-67-7    589-87-7    92-86-4    3988-03-2    35578-47-3 

[1]ChemistryLetters,1983,p.1201-1202

139-02-6    59696-27-4    108-86-1    101-55-3    101-84-8    591-50-4    589-87-7    71-43-2 

[1]JournaloftheAmericanChemicalSociety,1982,vol.104,p.3917-3923

19230-28-5    589-87-7    64258-06-6 

[1]JournaloftheAmericanChemicalSociety,1977,vol.99,p.5249-5253

589-87-7    100-52-7    29334-16-5 

[1]AngewandteChemie-InternationalEdition,1998,vol.37,p.1701-1703

Literature fold

Title: Copper-catalyzed one-pot multicomponent coupling reaction of phenols, amides, and 4-bromphenyl iodide.

Journal: Organic letters20081016

Title: Orientational isomerism and binding ability of nonsymmetrical guests encapsulated in a self-assembling heterodimeric capsule.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20050805

Title: Synthesis of N tau-arylhistidine derivatives via direct N-arylation.

Journal: Bioorganic & medicinal chemistry letters20040405

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