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2632-13-5,MFCD00000201
Catalog No.:AA00332N

2632-13-5 | 2-Bromo-4'-methoxyacetophenone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5mg
98%
in stock  
$6.00   $4.00
- +
25mg
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$11.00   $8.00
- +
10g
98%
in stock  
$13.00   $9.00
- +
25g
98%
in stock  
$29.00   $21.00
- +
100g
98%
in stock  
$72.00   $50.00
- +
  • Technical Information
  • Properties
  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00332N
Chemical Name:
2-Bromo-4'-methoxyacetophenone
CAS Number:
2632-13-5
Molecular Formula:
C9H9BrO2
Molecular Weight:
229.0706
MDL Number:
MFCD00000201
SMILES:
BrCC(=O)c1ccc(cc1)OC
NSC Number:
129010
Properties
Properties
 
BP:
306.7°C at 760 mmHg  
Form:
Solid  
MP:
69-72 °C  
Refractive Index:
1.5500 (estimate)  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
151  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
3  
XLogP3:
2.5  

Literature

Title: 6-Fluoro-2-(4-meth-oxy-phen-yl)imidazo[2,1-b][1,3]benzothia-zole.

Journal: Acta crystallographica. Section E, Structure reports online 20111201

Title: Switching reversibility to irreversibility in glycogen synthase kinase 3 inhibitors: clues for specific design of new compounds.

Journal: Journal of medicinal chemistry 20110623

Title: 2-Isobutyl-6-(4-meth-oxy-phen-yl)imidazo[2,1-b][1,3,4]thia-diazole.

Journal: Acta crystallographica. Section E, Structure reports online 20110201

Title: Effects of a fluorescent Myosin light chain phosphatase inhibitor on prostate cancer cells.

Journal: Frontiers in oncology 20110101

Title: 2-Bromo-1-(4-methoxy-phen-yl)ethanone.

Journal: Acta crystallographica. Section E, Structure reports online 20090901

Title: Thienyl and phenyl alpha-halomethyl ketones: new inhibitors of glycogen synthase kinase (GSK-3beta) from a library of compound searching.

Journal: Journal of medicinal chemistry 20031023

Title: alpha-bromoacetophenone derivatives as neutral protein tyrosine phosphatase inhibitors: structure-Activity relationship.

Journal: Bioorganic & medicinal chemistry letters 20021104

Title: Sylvest L, et al. Phosphatase inhibitors with anti-angiogenic effect in vitro. APMIS. 2010 Jan;118(1):49-59.

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