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Home Other Building Blocks 2-Bromo-4'-methoxyacetophenone

2-Bromo-4'-methoxyacetophenone

CAS No.:
2632-13-5
Catalog Number:
AG00335F
Molecular Formula:
C9H9BrO2
Molecular Weight:
229.0706
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$14
- +
25g
98%
In Stock USA
United States
$47
- +
100g
98%
In Stock USA
United States
$113
- +
500g
98%
In Stock USA
United States
$494
- +
Product Description
Catalog Number:
AG00335F
Chemical Name:
2-Bromo-4'-methoxyacetophenone
CAS Number:
2632-13-5
Molecular Formula:
C9H9BrO2
Molecular Weight:
229.0706
MDL Number:
MFCD00000201
IUPAC Name:
2-bromo-1-(4-methoxyphenyl)ethanone
InChI:
InChI=1S/C9H9BrO2/c1-12-8-4-2-7(3-5-8)9(11)6-10/h2-5H,6H2,1H3
InChI Key:
XQJAHBHCLXUGEP-UHFFFAOYSA-N
SMILES:
BrCC(=O)c1ccc(cc1)OC
EC Number:
220-118-8
NSC Number:
129010
Properties
Complexity:
151  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
227.979g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
229.073g/mol
Monoisotopic Mass:
227.979g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.5  
Literature
Title Journal
6-Fluoro-2-(4-meth-oxy-phen-yl)imidazo[2,1-b][1,3]benzothia-zole. Acta crystallographica. Section E, Structure reports online 20111201
Switching reversibility to irreversibility in glycogen synthase kinase 3 inhibitors: clues for specific design of new compounds. Journal of medicinal chemistry 20110623
2-Isobutyl-6-(4-meth-oxy-phen-yl)imidazo[2,1-b][1,3,4]thia-diazole. Acta crystallographica. Section E, Structure reports online 20110201
Effects of a fluorescent Myosin light chain phosphatase inhibitor on prostate cancer cells. Frontiers in oncology 20110101
2-Bromo-1-(4-methoxy-phen-yl)ethanone. Acta crystallographica. Section E, Structure reports online 20090901
Thienyl and phenyl alpha-halomethyl ketones: new inhibitors of glycogen synthase kinase (GSK-3beta) from a library of compound searching. Journal of medicinal chemistry 20031023
alpha-bromoacetophenone derivatives as neutral protein tyrosine phosphatase inhibitors: structure-Activity relationship. Bioorganic & medicinal chemistry letters 20021104
Properties