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Home Bromides 50530-12-6
50530-12-6,MFCD00014388
Catalog No.:AA003DRB

50530-12-6 | 10-Bromodecanoic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$8.00   $6.00
- +
5g
95%
in stock  
$11.00   $8.00
- +
10g
95%
in stock  
$13.00   $9.00
- +
25g
95%
in stock  
$29.00   $21.00
- +
100g
95%
in stock  
$75.00   $53.00
- +
500g
95%
in stock  
$342.00   $239.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003DRB
Chemical Name:
10-Bromodecanoic acid
CAS Number:
50530-12-6
Molecular Formula:
C10H19BrO2
Molecular Weight:
251.1607
MDL Number:
MFCD00014388
SMILES:
BrCCCCCCCCCC(=O)O
Properties
Properties
 
BP:
339.2°C at 760 mmHg  
Form:
Solid  
MP:
38-41 °C(lit.)  
Refractive Index:
1.5845 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
126  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
9  
XLogP3:
4  

Upstream Synthesis Route

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1993,#10,p.1183-1190

[1]JournalofOrganicChemistry,1970,vol.35,p.4241-4244

[1]BioorganicandMedicinalChemistry,2011,vol.19,#1,p.567-579

[2]Patent:DE867243,1943,,

[3]JournaloftheAmericanChemicalSociety,1956,vol.78,p.2255,2256

[4]JournalofOrganicChemistry,1956,vol.21,p.883,885

[5]MolecularCrystalsandLiquidCrystalsScienceandTechnology,SectionA:MolecularCrystalsandLiquidCrystals,2000,vol.350,p.93-101

[6]BioorganicandMedicinalChemistry,2018,vol.26,#14,p.4001-4013

[1]Patent:WO2018/80869,2018,A1,.Locationinpatent:Paragraph0084

[1]JournalofOrganicChemistry,1991,vol.56,#17,p.5132-5138

[2]JournalofMaterialsChemistry,1999,vol.9,#10,p.2399-2405

[3]HelveticaChimicaActa,1926,vol.9,p.1086

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.PerkintransactionsI,1993,p.1183-1190

[2]HelveticaChimicaActa,1929,vol.12,p.478

[3]JournaloftheChemicalSociety,1949,p.1548

[4]HelveticaChimicaActa,1974,vol.57,p.434-440

[1]JournalofMedicinalChemistry,2012,vol.55,p.7163-7172

[2]JournaloftheChemicalSociety,1949,p.1475

[3]ACSChemicalNeuroscience,2017,vol.8,p.1949-1959

[1]BioorganicandMedicinalChemistry,2011,vol.19,p.567-579

[2]Patent:DE867243,1943,

[3]JournaloftheAmericanChemicalSociety,1956,vol.78,p.2255,2256    JournalofOrganicChemistry,1956,vol.21,p.883,885

[4]MolecularCrystalsandLiquidCrystalsScienceandTechnology,SectionA:MolecularCrystalsandLiquidCrystals,2000,vol.350,p.93-101

[5]BioorganicandMedicinalChemistry,2018,vol.26,p.4001-4013

[1]Patent:WO2011/6061,2011,A1.Locationinpatent:Page/Pagecolumn44-45

[2]JournaloftheChemicalSociety.PerkintransactionsI,1993,p.1183-1190

[3]ChemischeBerichte,1942,vol.75,p.294

[1]JournalofOrganicChemistry,1991,vol.56,p.5132-5138

[2]Langmuir,2012,vol.28,p.14172-14179,8

[3]Patent:WO2009/77844,2009,A2.Locationinpatent:Page/Pagecolumn71-72

[4]BioorganicandMedicinalChemistry,1997,vol.5,p.1267-1274

[5]HelveticaChimicaActa,1974,vol.57,p.434-440

Literature

Title: Design, synthesis and antimycobacterial activities of 1-methyl-2-alkenyl-4(1H)-quinolones.

Journal: Bioorganic & medicinal chemistry 20110101

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SDS
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