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Home Bromides 30515-28-7
30515-28-7,MFCD00037800
Catalog No.:AA0030C5

30515-28-7 | 7-Bromoheptanoic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$7.00   $5.00
- +
5g
97%
in stock  
$12.00   $8.00
- +
10g
98%
in stock  
$15.00   $10.00
- +
25g
98%
in stock  
$29.00   $20.00
- +
  • 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:
AA0030C5
Chemical Name:
7-Bromoheptanoic acid
CAS Number:
30515-28-7
Molecular Formula:
C7H13BrO2
Molecular Weight:
209.0809
MDL Number:
MFCD00037800
SMILES:
BrCCCCCCC(=O)O
Properties
Computed Properties
 
Complexity:
93.6  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
6  
XLogP3:
1  

Upstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,1998,vol.8,#22,p.3281-3286

[1]ChemischeBerichte,1906,vol.39,p.4364

[1]JournalofNaturalProducts,2016,vol.79,#1,p.244-247

[2]TetrahedronLetters,2012,vol.53,#24,p.3082-3085

[3]BioorganicandMedicinalChemistry,2013,vol.21,#22,p.6981-6995

[4]InorganicChemistry,2017,vol.56,#18,p.11050-11058

[1]BulletinoftheChemicalSocietyofJapan,1986,vol.59,#11,p.3535-3539

[1]TetrahedronLetters,2012,vol.53,#24,p.3082-3085

Downstream Synthesis Route

[1]JournaloftheChemicalSociety,1950,p.174,176

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

[3]ChineseJournalofChemistry,2014,vol.32,p.157-162

[4]Patent:WO2014/78895,2014,A1.Locationinpatent:Page/Pagecolumn23;38

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

[6]Tetrahedron,2017,vol.73,p.6275-6285

[1]Patent:WO2012/96832,2012,A2.Locationinpatent:Page/Pagecolumn37

[2]Macromolecules,2004,vol.37,p.8286-8292

[3]JournaloftheChemicalSociety,1961,p.2404-2418

[4]MolecularCrystalsandLiquidCrystals(1969-1991),1990,vol.182,p.201-207

[5]JournalofOrganicChemistry,1993,vol.58,p.1290-1292

[6]RecueildesTravauxChimiquesdesPays-Bas,1992,vol.111,p.421-426

[7]JournalofMedicinalChemistry,2005,vol.48,p.1019-1032

[8]BioorganicandMedicinalChemistryLetters,2005,vol.15,p.331-335

[9]JournalofMedicinalChemistry,2008,vol.51,p.1894-1903

[10]BioorganicandMedicinalChemistry,2010,vol.18,p.605-611

[11]JournalofMedicinalChemistry,2010,vol.53,p.5629-5638

[12]EuropeanJournalofMedicinalChemistry,2016,vol.108,p.730-740

[13]Patent:JP5839317,2016,B2.Locationinpatent:Paragraph0054

[14]BioorganicChemistry,2018,vol.81,p.373-381

[1]EuropeanJournalofOrganicChemistry,2013,p.1716-1725

[2]JournaloftheChemicalSociety,1963,p.5889-5893

[1]NewJournalofChemistry,2018,vol.42,p.8765-8772

[2]Tetrahedron,2015,vol.71,p.3939-3945

[3]MolecularCrystalsandLiquidCrystalsScienceandTechnology,SectionA:MolecularCrystalsandLiquidCrystals,1993,vol.225,p.269-278

Literature

Title: Enantioselective synthesis of pentacycloanammoxic acid.

Journal: Journal of the American Chemical Society 20060315

Title: Total synthesis of (+/-)-pentacycloanammoxic acid.

Journal: Journal of the American Chemical Society 20041208

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SDS
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