Home Boronic acids 4-Methoxyphenylboronic acid

4-Methoxyphenylboronic acid

CAS No.:
5720-07-0
Catalog Number:
AG00343C
Molecular Formula:
C7H9BO3
Molecular Weight:
151.9556
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$8
- +
25g
95%
In Stock USA
United States
$20
- +
100g
95%
In Stock USA
United States
$63
- +
Product Description
Catalog Number:
AG00343C
Chemical Name:
4-Methoxyphenylboronic acid
CAS Number:
5720-07-0
Molecular Formula:
C7H9BO3
Molecular Weight:
151.9556
MDL Number:
MFCD00039139
IUPAC Name:
(4-methoxyphenyl)boronic acid
InChI:
InChI=1S/C7H9BO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3
InChI Key:
VOAAEKKFGLPLLU-UHFFFAOYSA-N
SMILES:
COc1ccc(cc1)B(O)O
EC Number:
611-482-2
Properties
Complexity:
110  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
152.064g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
151.956g/mol
Monoisotopic Mass:
152.064g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
49.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
Gold- and silver-catalyzed reactions of propargylic alcohols in the presence of protic additives. Chemistry (Weinheim an der Bergstrasse, Germany) 20120410
A general procedure for the synthesis of enones via gold-catalyzed Meyer-Schuster rearrangement of propargylic alcohols at room temperature. The Journal of organic chemistry 20110304
Expanding stereochemical and skeletal diversity using petasis reactions and 1,3-dipolar cycloadditions. Organic letters 20101119
Aryl boronic acid inhibition of synthetic melanin polymerization. Bioorganic & medicinal chemistry letters 20100801
Improved syntheses of morinol C and D by employing Mizoroki-Heck reaction and their cytotoxic and antimicrobial activities. Bioscience, biotechnology, and biochemistry 20100101
Metal-free carbon-carbon bond-forming reductive coupling between boronic acids and tosylhydrazones. Nature chemistry 20090901
Discovery of boronic acids as novel and potent inhibitors of fatty acid amide hydrolase. Journal of medicinal chemistry 20081127
Synthesis of 2,6-diphenylpyrazine derivatives and their DNA binding and cytotoxic properties. European journal of medicinal chemistry 20051201
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. Inorganic chemistry 20020812
Properties