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5720-07-0,MFCD00039139
Catalog No.:AA00340K

5720-07-0 | 4-Methoxyphenylboronic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
99%
in stock  
$6.00   $4.00
- +
5g
99%
in stock  
$9.00   $6.00
- +
10g
99%
in stock  
$12.00   $8.00
- +
25g
99%
in stock  
$13.00   $9.00
- +
100g
99%
in stock  
$30.00   $21.00
- +
500g
99%
in stock  
$149.00   $104.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00340K
Chemical Name:
4-Methoxyphenylboronic acid
CAS Number:
5720-07-0
Molecular Formula:
C7H9BO3
Molecular Weight:
151.9556
MDL Number:
MFCD00039139
SMILES:
COc1ccc(cc1)B(O)O
Properties
Properties
 
BP:
306.8°C at 760 mmHg  
Form:
Solid  
MP:
204-206 °C(lit.)  
Solubility:
Soluble in dimethyl sulfoxide and methanol.  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
110  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  

Literature

Title: Gold- and silver-catalyzed reactions of propargylic alcohols in the presence of protic additives.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20120410

Title: A general procedure for the synthesis of enones via gold-catalyzed Meyer-Schuster rearrangement of propargylic alcohols at room temperature.

Journal: The Journal of organic chemistry 20110304

Title: Expanding stereochemical and skeletal diversity using petasis reactions and 1,3-dipolar cycloadditions.

Journal: Organic letters 20101119

Title: Aryl boronic acid inhibition of synthetic melanin polymerization.

Journal: Bioorganic & medicinal chemistry letters 20100801

Title: Improved syntheses of morinol C and D by employing Mizoroki-Heck reaction and their cytotoxic and antimicrobial activities.

Journal: Bioscience, biotechnology, and biochemistry 20100101

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

Journal: Nature chemistry 20090901

Title: Discovery of boronic acids as novel and potent inhibitors of fatty acid amide hydrolase.

Journal: Journal of medicinal chemistry 20081127

Title: Synthesis of 2,6-diphenylpyrazine derivatives and their DNA binding and cytotoxic properties.

Journal: European journal of medicinal chemistry 20051201

Title: Tetraarylpentaborates, [B(5)O(6)Ar(4)](-) (Ar = C(6)H(4)OMe-4, C(6)H(3)Me(2)-2,6): their formation from the reaction of arylboronic acids with an aryloxorhodium complex, structure, and chemical properties.

Journal: Inorganic chemistry 20020812

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SDS
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Tags:5720-07-0 Molecular Formula|5720-07-0 MDL|5720-07-0 SMILES|5720-07-0 4-Methoxyphenylboronic acid
Catalog No.: AA00340K
5720-07-0,MFCD00039139
5720-07-0 | 4-Methoxyphenylboronic acid
Pack Size： 1g
Purity： 99%
in stock
$6.00 $4.00
Pack Size： 5g
Purity： 99%
in stock
$9.00 $6.00
Pack Size： 10g
Purity： 99%
in stock
$12.00 $8.00
Pack Size： 25g
Purity： 99%
in stock
$13.00 $9.00
Pack Size： 100g
Purity： 99%
in stock
$30.00 $21.00
Pack Size： 500g
Purity： 99%
in stock
$149.00 $104.00
Quantity
- +
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Technical Information
Catalog Number: AA00340K
Chemical Name: 4-Methoxyphenylboronic acid
CAS Number: 5720-07-0
Molecular Formula: C7H9BO3
Molecular Weight: 151.9556
MDL Number: MFCD00039139
SMILES: COc1ccc(cc1)B(O)O
Properties
BP: 306.8°C at 760 mmHg  
Form: Solid  
MP: 204-206 °C(lit.)  
Solubility: Soluble in dimethyl sulfoxide and methanol.  
Storage: Keep in dry area;2-8℃;  
Complexity: 110  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  
Literature fold

Title: Gold- and silver-catalyzed reactions of propargylic alcohols in the presence of protic additives.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20120410

Title: A general procedure for the synthesis of enones via gold-catalyzed Meyer-Schuster rearrangement of propargylic alcohols at room temperature.

Journal: The Journal of organic chemistry20110304

Title: Expanding stereochemical and skeletal diversity using petasis reactions and 1,3-dipolar cycloadditions.

Journal: Organic letters20101119

Title: Aryl boronic acid inhibition of synthetic melanin polymerization.

Journal: Bioorganic & medicinal chemistry letters20100801

Title: Improved syntheses of morinol C and D by employing Mizoroki-Heck reaction and their cytotoxic and antimicrobial activities.

Journal: Bioscience, biotechnology, and biochemistry20100101

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

Journal: Nature chemistry20090901

Title: Discovery of boronic acids as novel and potent inhibitors of fatty acid amide hydrolase.

Journal: Journal of medicinal chemistry20081127

Title: Synthesis of 2,6-diphenylpyrazine derivatives and their DNA binding and cytotoxic properties.

Journal: European journal of medicinal chemistry20051201

Title: Tetraarylpentaborates, [B(5)O(6)Ar(4)](-) (Ar = C(6)H(4)OMe-4, C(6)H(3)Me(2)-2,6): their formation from the reaction of arylboronic acids with an aryloxorhodium complex, structure, and chemical properties.

Journal: Inorganic chemistry20020812

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