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5467-74-3,MFCD00002104
Catalog No.:AA003KY7

5467-74-3 | 4-Bromophenylboronic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
>97%
in stock  
$10.00   $7.00
- +
25g
95%
in stock  
$40.00   $28.00
- +
100g
>97%
in stock  
$64.00   $45.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003KY7
Chemical Name:
4-Bromophenylboronic acid
CAS Number:
5467-74-3
Molecular Formula:
C6H6BBrO2
Molecular Weight:
200.8256
MDL Number:
MFCD00002104
SMILES:
OB(c1ccc(cc1)Br)O
NSC Number:
25407
Properties
Properties
 
BP:
315°C at 760 mmHg  
Form:
Solid  
MP:
280 °C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
102  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Literature

Title: Synthesis of functionalized cinnamaldehyde derivatives by an oxidative Heck reaction and their use as starting materials for preparation of Mycobacterium tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase inhibitors.

Journal: The Journal of organic chemistry 20111104

Title: Enhanced effect and mechanism of water-in-oil microemulsion as an oral delivery system of hydroxysafflor yellow A.

Journal: International journal of nanomedicine 20110101

Title: Inhibition studies of soybean (Glycine max) urease with heavy metals, sodium salts of mineral acids, boric acid, and boronic acids.

Journal: Journal of enzyme inhibition and medicinal chemistry 20101001

Title: Phenylboronic-acid-based carbohydrate binders as antiviral therapeutics: monophenylboronic acids.

Journal: Antiviral chemistry & chemotherapy 20100811

Title: Aryl boronic acid inhibition of synthetic melanin polymerization.

Journal: Bioorganic & medicinal chemistry letters 20100801

Title: Metal-free carbon-carbon bond-forming reductive coupling between boronic acids and tosylhydrazones.

Journal: Nature chemistry 20090901

Title: Boric acid and boronic acids inhibition of pigeonpea urease.

Journal: Journal of enzyme inhibition and medicinal chemistry 20060801

Title: Continuous monitoring of arylesterase in human serum.

Journal: Clinica chimica acta; international journal of clinical chemistry 20010601

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SDS
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Tags:5467-74-3 Molecular Formula|5467-74-3 MDL|5467-74-3 SMILES|5467-74-3 4-Bromophenylboronic acid
Catalog No.: AA003KY7
5467-74-3,MFCD00002104
5467-74-3 | 4-Bromophenylboronic acid
Pack Size： 5g
Purity： >97%
in stock
$10.00 $7.00
Pack Size： 25g
Purity： 95%
in stock
$40.00 $28.00
Pack Size： 100g
Purity： >97%
in stock
$64.00 $45.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003KY7
Chemical Name: 4-Bromophenylboronic acid
CAS Number: 5467-74-3
Molecular Formula: C6H6BBrO2
Molecular Weight: 200.8256
MDL Number: MFCD00002104
SMILES: OB(c1ccc(cc1)Br)O
NSC Number: 25407
Properties
BP: 315°C at 760 mmHg  
Form: Solid  
MP: 280 °C  
Storage: Keep in dry area;2-8℃;  
Complexity: 102  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Literature fold

Title: Synthesis of functionalized cinnamaldehyde derivatives by an oxidative Heck reaction and their use as starting materials for preparation of Mycobacterium tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase inhibitors.

Journal: The Journal of organic chemistry20111104

Title: Enhanced effect and mechanism of water-in-oil microemulsion as an oral delivery system of hydroxysafflor yellow A.

Journal: International journal of nanomedicine20110101

Title: Inhibition studies of soybean (Glycine max) urease with heavy metals, sodium salts of mineral acids, boric acid, and boronic acids.

Journal: Journal of enzyme inhibition and medicinal chemistry20101001

Title: Phenylboronic-acid-based carbohydrate binders as antiviral therapeutics: monophenylboronic acids.

Journal: Antiviral chemistry & chemotherapy20100811

Title: Aryl boronic acid inhibition of synthetic melanin polymerization.

Journal: Bioorganic & medicinal chemistry letters20100801

Title: Metal-free carbon-carbon bond-forming reductive coupling between boronic acids and tosylhydrazones.

Journal: Nature chemistry20090901

Title: Boric acid and boronic acids inhibition of pigeonpea urease.

Journal: Journal of enzyme inhibition and medicinal chemistry20060801

Title: Continuous monitoring of arylesterase in human serum.

Journal: Clinica chimica acta; international journal of clinical chemistry20010601

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