Home Bromides 1200-03-9
1200-03-9,MFCD00000262
Catalog No.:AA000PYE

1200-03-9 | 4-Phenoxybutyl bromide

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1g
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$8.00   $6.00
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5g
97%
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$17.00   $12.00
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25g
97%
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$58.00   $41.00
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100g
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500g
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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:
AA000PYE
Chemical Name:
4-Phenoxybutyl bromide
CAS Number:
1200-03-9
Molecular Formula:
C10H13BrO
Molecular Weight:
229.1136
MDL Number:
MFCD00000262
SMILES:
BrCCCCOc1ccccc1
NSC Number:
17155
Properties
Computed Properties
 
Complexity:
100  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
5  
XLogP3:
3.8  

Upstream Synthesis Route

[1]Patent:CN104447220,2016,B,.Locationinpatent:Paragraph0024-0026

[2]ArchivderPharmazie,2009,vol.342,#12,p.732-739

[3]BioorganicandMedicinalChemistry,2010,vol.18,#3,p.1244-1251

[4]TetrahedronLetters,2010,vol.51,#35,p.4612-4616

[5]ChemicalCommunications,2014,vol.50,#39,p.5017-5019

[6]OrganicPreparationsandProceduresInternational,2003,vol.35,#5,p.501-507

[7]Chemistry-AEuropeanJournal,2017,vol.23,#60,p.15041-15045

[8]Patent:WO2010/146112,2010,A1,.Locationinpatent:Page/Pagecolumn111

[9]JournalofOrganicChemistry,1956,vol.21,p.61,63

[10]Patent:US2603656,1951,,

[11]BulletindelaSocieteChimiquedeFrance,1950,p.1062

[12]AnnalesPharmaceutiquesFrancaises,1952,vol.10,p.181,186

[13]JournalofMedicinalChemistry,1965,vol.8,p.271-273

[14]JournalofOrganicChemistry,1962,vol.27,p.1288-1294

[15]ChemistryofHeterocyclicCompounds,2003,vol.39,#9,p.1218-1226

[16]PharmacyandPharmacologyCommunications,1999,vol.5,#8,p.491-494

[17]EuropeanJournalofMedicinalChemistry,2009,vol.44,#10,p.4218-4226

[18]BioorganicandMedicinalChemistry,2013,vol.21,#17,p.5145-5153

[19]ChineseJournalofChemistry,2015,vol.33,#3,p.384-388

[20]InorganicaChimicaActa,2015,vol.433,p.63-71

[21]Chemico-BiologicalInteractions,2016,vol.259,p.154-159

[22]Patent:WO2017/9651,2017,A1,.Locationinpatent:Page/Pagecolumn84

[1]Molecules,2018,vol.23,#11,

[1]Patent:US4380546,1983,A,

[2]Patent:US4456608,1984,A,

[1]JournaloftheAmericanChemicalSociety,1922,vol.44,p.2649

[2]JournalofOrganicChemistry,1968,vol.33,#6,p.2271-2284

[1]JournaloftheIndianInstituteofScience,1923,vol.6,p.54

[2]Chem.Zentralbl.,1923,vol.94,#III,p.997

[3]JournaloftheAmericanChemicalSociety,1922,vol.44,p.2649

Downstream Synthesis Route

[1]Weiske,Thomas;Schwarz,Helmut[ChemischeBerichte,1983,vol.116,#1,p.323-347]

[2]Diekman,J.etal.[JournalofOrganicChemistry,1968,vol.33,#6,p.2271-2284]

[3]Burns,TimothyP.;Rieke,ReubenD.[JournalofOrganicChemistry,1983,vol.48,#22,p.4141-4143]

[1]WINTERFELD;MEYER[ArchivderPharmazie,1961,vol.294/66,p.630-639]

[1]Imam;Devinsky;Lacko;Mlynarcik;Krasnec[Pharmazie,1983,vol.38,#5,p.308-310]

132205-64-2    1200-03-9   
1-Cyano-1-(4-phenoxybutyl)-tetralin 

[1]ArchivderPharmazie,1989,vol.322,p.889-892

[1]MolecularPharmacology,2005,vol.68,p.1254-1270

[2]Patent:US2006/79535,2006,A1.Locationinpatent:Page/Pagecolumn4-5

Literature
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SDS
Tags:1200-03-9 Molecular Formula|1200-03-9 MDL|1200-03-9 SMILES|1200-03-9 4-Phenoxybutyl bromide