Home Boronic Acids 4426-47-5
4426-47-5,MFCD00002106
Catalog No.:AA0034HY

4426-47-5 | n-Butylboronic acid

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1g
95%
in stock  
$18.00   $13.00
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5g
96%
in stock  
$29.00   $20.00
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25g
96%
in stock  
$62.00   $44.00
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100g
96%
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$157.00   $110.00
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500g
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$726.00   $509.00
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  • 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:
AA0034HY
Chemical Name:
n-Butylboronic acid
CAS Number:
4426-47-5
Molecular Formula:
C4H11BO2
Molecular Weight:
101.9399
MDL Number:
MFCD00002106
SMILES:
CCCCB(O)O
Properties
Properties
 
BP:
189.2°C at 760 mmHg  
Form:
Liquid  
MP:
90-92 °C(lit.)  
Stability:
Air Sensitive & Hygroscopic  
Storage:
-20 ℃;Light sensitive;  

Computed Properties
 
Complexity:
38.7  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
3  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2012,vol.134,#27,p.11298-11298

[2]ChemicalCommunications,2012,vol.48,#9,p.1230-1232

[3]BioorganicandMedicinalChemistryLetters,2002,vol.12,#21,p.3199-3202

[4]JournaloftheAmericanChemicalSociety,2017,vol.139,#8,p.3153-3160

[1]Organometallics,1983,vol.2,p.230-236

[1]OrganicandBiomolecularChemistry,2005,vol.3,#5,p.941-944

[1]OrganicandBiomolecularChemistry,2005,vol.3,#5,p.941-944

Downstream Synthesis Route
22348-32-9    4426-47-5   
(S)-tetrahydro-1-butyl-3,3-diphenyl-1H,3H-pyrrolo{2,1-c}{1,3,2}oxazaborole 

[1]HelveticaChimicaActa,2001,vol.84,p.431-472

[2]JournaloftheAmericanChemicalSociety,2007,vol.129,p.10346-10347

[3]OrganicLetters,2009,vol.11,p.1611-1614

[4]Patent:US2004/198701,2004,A1.Locationinpatent:Page/Pagecolumn16

[5]Patent:US2005/227969,2005,A1.Locationinpatent:Page/Pagecolumn17

4426-47-5    210298-83-2   
6-butyl-3,4-dihydro-2H-pyridine-1-carboxylicacidbenzylester 

[1]JournalofOrganicChemistry,2001,vol.66,p.2459-2465

4426-47-5    171288-01-0   
6-butyl-3,4-dihydro-2H-pyridine-1-carboxylicacidtert-butylester 

[1]JournalofOrganicChemistry,2001,vol.66,p.2459-2465

[1]JournalofOrganicChemistry,2008,vol.73,p.8448-8451

[2]JournalofOrganicChemistry,2012,vol.77,p.2729-2742

[3]Tetrahedron,2004,vol.60,p.3813-3818

[4]TetrahedronLetters,2009,vol.50,p.1003-1006

[5]TetrahedronLetters,2001,vol.42,p.7213-7215

[6]JournalofOrganometallicChemistry,2009,vol.694,p.1658-1665

[7]Chemistry-AEuropeanJournal,2003,vol.9,p.3216-3227

[8]Organometallics,2011,vol.30,p.4393-4403

[1]JournalofOrganicChemistry,2002,vol.67,p.5553-5566

[2]ChemicalCommunications,2004,p.2336-2337

[3]Tetrahedron,2004,vol.60,p.3813-3818

Literature

Title: Inhibition studies of soybean (Glycine max) urease with heavy metals, sodium salts of mineral acids, boric acid, and boronic acids.

Journal: Journal of enzyme inhibition and medicinal chemistry 20101001

Title: Inhibitors of bacterial N-succinyl-L,L-diaminopimelic acid desuccinylase (DapE) and demonstration of in vitro antimicrobial activity.

Journal: Bioorganic & medicinal chemistry letters 20091115

Title: Structural and spectroscopic properties of an aliphatic boronic acid studied by combination of experimental and theoretical methods.

Journal: The Journal of chemical physics 20080328

Title: Carbohydrate supplementation during prolonged cycling exercise spares muscle glycogen but does not affect intramyocellular lipid use.

Journal: Pflugers Archiv : European journal of physiology 20070701

Title: Boric acid and boronic acids inhibition of pigeonpea urease.

Journal: Journal of enzyme inhibition and medicinal chemistry 20060801

Title: Both nucleophile and substrate bind to the catalytic Fe(II)-center in the type-II methionyl aminopeptidase from Pyrococcus furiosus.

Journal: Inorganic chemistry 20050307

Title: Sensitive and simple determination of mannitol in human brain tissues by gas chromatography-mass spectrometry.

Journal: Journal of chromatography. B, Biomedical sciences and applications 20010705

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