Home Bromides 459-46-1
459-46-1,MFCD00000359
Catalog No.:AA0033YM

459-46-1 | 4-Fluorobenzyl Bromide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%(GC)
in stock  
$24.00   $17.00
- +
5g
98%(GC)
in stock  
$35.00   $25.00
- +
25g
>97.0%(GC)
in stock  
$103.00   $72.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0033YM
Chemical Name:
4-Fluorobenzyl Bromide
CAS Number:
459-46-1
Molecular Formula:
C7H6BrF
Molecular Weight:
189.0249
MDL Number:
MFCD00000359
SMILES:
BrCc1ccc(cc1)F
Properties
Properties
 
BP:
223.5°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.547(lit.)  
Stability:
Lachrymatory  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
77  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.8  

Literature

Title: N-[3-(4-Fluoro-benz-yl)-2,4-dioxo-1,3-diaza-spiro-[4.5]dec-8-yl]-2-methyl-benzene-sulfonamide.

Journal: Acta crystallographica. Section E, Structure reports online 20120101

Title: Structure-based design of novel boronic acid-based inhibitors of autotaxin.

Journal: Journal of medicinal chemistry 20110714

Title: Distributed Drug Discovery, Part 3: using D(3) methodology to synthesize analogs of an anti-melanoma compound.

Journal: Journal of combinatorial chemistry 20090112

Title: Distributed Drug Discovery, Part 2: global rehearsal of alkylating agents for the synthesis of resin-bound unnatural amino acids and virtual D(3) catalog construction.

Journal: Journal of combinatorial chemistry 20090112

Title: Novel quinolinonyl diketo acid derivatives as HIV-1 integrase inhibitors: design, synthesis, and biological activities.

Journal: Journal of medicinal chemistry 20080814

Title: Human immunodeficiency virus integrase inhibitors efficiently suppress feline immunodeficiency virus replication in vitro and provide a rationale to redesign antiretroviral treatment for feline AIDS.

Journal: Retrovirology 20070101

Title: Synthesis of new glycyrrhetinic acid (GA) derivatives and their effects on tyrosinase activity.

Journal: Bioorganic & medicinal chemistry 20031201

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SDS
Tags:459-46-1 Molecular Formula|459-46-1 MDL|459-46-1 SMILES|459-46-1 4-Fluorobenzyl Bromide |Fluorinated_Building_Blocks