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Home Bromides 4654-39-1
4654-39-1,MFCD00002897
Catalog No.:AA003THE

4654-39-1 | 2-(4-Bromophenyl)ethanol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$9.00   $7.00
- +
10g
98%
in stock  
$16.00   $11.00
- +
25g
98%
in stock  
$33.00   $23.00
- +
100g
98%
in stock  
$121.00   $85.00
- +
500g
98%
in stock  
$579.00   $405.00
- +
  • 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:
AA003THE
Chemical Name:
2-(4-Bromophenyl)ethanol
CAS Number:
4654-39-1
Molecular Formula:
C8H9BrO
Molecular Weight:
201.0605
MDL Number:
MFCD00002897
SMILES:
OCCc1ccc(cc1)Br
Properties
Properties
 
BP:
274.6°C at 760 mmHg  
Form:
Liquid  
MP:
36-38 °C(lit.)  
Refractive Index:
n20/D 1.573(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
87.3  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
1.5  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2014,vol.136,#7,p.2711-2714

[2]Patent:WO2005/63239,2005,A1,.Locationinpatent:Page/Pagecolumn134

[1]BioorganicandMedicinalChemistryLetters,2008,vol.18,#14,p.4199-4203

[1]OrganicProcessResearchandDevelopment,2006,vol.10,#5,p.1076-1079

[1]JournalofMedicinalChemistry,2012,vol.55,#11,p.5627-5631

[2]Patent:WO2015/66413,2015,A1,.Locationinpatent:Page/Pagecolumn164;165

[3]Chemistry-AEuropeanJournal,2015,vol.21,#42,p.14737-14741

[4]AdvancedSynthesisandCatalysis,2012,vol.354,#10,p.1879-1884

[5]Synthesis,2011,#18,p.2935-2940

[1]BioorganicandMedicinalChemistry,2013,vol.21,#12,p.3465-3472

[2]OrganicandBiomolecularChemistry,2010,vol.8,#15,p.3552-3562

[3]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1977,p.2357-2364

Downstream Synthesis Route

[1]JournalofOrganometallicChemistry,2015,vol.776,p.153-156

[2]JournalofChemicalSciences,2016,vol.128,p.1695-1701

[3]Patent:CN106478506,2017,A.Locationinpatent:Paragraph0133;0134

[4]Patent:US2002/19531,2002,A1

[5]Patent:US2862971,1955,

[6]JournaloftheChemicalSociety.PerkintransactionsI,1977,p.2357-2364

[7]JournalofOrganicChemistry,1964,vol.29,p.2109-2116

[8]Tetrahedron,1990,vol.46,p.7247-7262

[9]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.4752-4756

[10]Patent:US5942544,1999,A

[11]Patent:EP892780,2002,B1

[12]Patent:US2005/137236,2005,A1.Locationinpatent:Page/Pagecolumn20

[13]AngewandteChemie-InternationalEdition,2020,vol.59,p.1129-1133    Angew.Chem.,2019,vol.132,p.1145-1149,5

[1]JournaloftheAmericanChemicalSociety,1948,vol.70,p.4177

[1]Sowa,Sylwia;Mühlberg,Michaela;Pietrusiewicz,K.Michal;Hackenberger,ChristianP.R.[BioorganicandMedicinalChemistry,2013,vol.21,#12,p.3465-3472]

[2]Locationinpatent:experimentalpartSchuepbach,Bjoern;Terfort,Andreas[OrganicandBiomolecularChemistry,2010,vol.8,#15,p.3552-3562]

[3]Davies,R.V.etal.[JournaloftheChemicalSociety.PerkintransactionsI,1977,p.2357-2364]

[1]OrganicLetters,2012,vol.14,p.696-699

[2]Patent:WO2020/14332,2020,A1.Locationinpatent:Paragraph00284;00298;00374

[3]Tetrahedron,1992,vol.48,p.10233-10238

[4]Patent:CN106565467,2017,A.Locationinpatent:Paragraph0044;0045

[5]Journaloflabelledcompoundsandradiopharmaceuticals,1994,vol.34,p.537-544

[6]JournaloftheAmericanChemicalSociety,2006,vol.128,p.14800-14801

[7]EuropeanJournalofInorganicChemistry,2011,p.2238-2246

[8]PeptideScience,2018,vol.110

[9]TetrahedronAsymmetry,1993,vol.4,p.2183-2198

[10]ChemicalResearchinToxicology,1996,vol.9,p.445-450

[11]Tetrahedron,1983,vol.39,p.2531-2549

[12]Patent:EP2196465,2010,A1.Locationinpatent:Page/Pagecolumn39

[13]Chemistry-AEuropeanJournal,2011,vol.17,p.13349-13357

[14]JournaloftheAmericanChemicalSociety,1996,vol.118,p.5881-5890

[15]TetrahedronLetters,1990,vol.31,p.6553-6556

[16]JournaloftheAmericanChemicalSociety,1995,vol.117,p.12159-12171

[17]Patent:WO2007/14462,2007,A1.Locationinpatent:Page/Pagecolumn18-19

[18]Patent:EP1961744,2008,A1.Locationinpatent:Page/Pagecolumn154

[19]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.4199-4203

[20]Patent:WO2009/9122,2009,A2.Locationinpatent:Page/Pagecolumn73

[21]Patent:US6790842,2004,B1.Locationinpatent:Page/Pagecolumn19

[22]Patent:WO2011/89416,2011,A1.Locationinpatent:Page/Pagecolumn88

[23]Polymer,2013,vol.54,p.269-276

[1]Patent:WO2008/5338,2008,A1.Locationinpatent:Page/Pagecolumn62-63

[2]Patent:WO2008/48609,2008,A1.Locationinpatent:Page/Pagecolumn53-54

[3]Patent:US9586928,2017,B2.Locationinpatent:Page/Pagecolumn155

[4]Patent:WO2009/105206,2009,A1.Locationinpatent:Page/Pagecolumn98

[5]CarbohydrateResearch,2003,vol.338,p.29-34

[6]JournalofMedicinalChemistry,2016,vol.59,p.7801-7817

[7]JournaloftheAmericanChemicalSociety,2007,vol.129,p.11421-11430

[8]Patent:US8410247,2013,B2.Locationinpatent:Page/Pagecolumn25;32

[9]BioorganicandMedicinalChemistry,2013,vol.21,p.3465-3472

[10]BioorganicandMedicinalChemistry,1996,vol.4,p.645-654

[11]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.4133-4136

[12]JournalofMedicinalChemistry,1989,vol.32,p.1108-1118

[13]JournaloftheChemicalSociety.PerkintransactionsI,1995,p.1273-1280

[14]Patent:WO2005/14525,2005,A2.Locationinpatent:Page/Pagecolumn43;44

[15]JournalofMedicinalChemistry,2009,vol.52,p.5603-5611

[16]JournalofMedicinalChemistry,2010,vol.53,p.3154-3168

[17]BioorganicandMedicinalChemistryLetters,2012,vol.22,p.71-75

[18]Patent:US2013/197217,2013,A1.Locationinpatent:Paragraph0586

[19]Patent:WO2014/26657,2014,A2.Locationinpatent:Page/Pagecolumn12

[20]Patent:EP2772482,2014,A1.Locationinpatent:Paragraph0274;0275

[21]Patent:WO2009/151598,2009,A1.Locationinpatent:Page/Pagecolumn147-148

[22]AngewandteChemie-InternationalEdition,2020,vol.59,p.1129-1133    Angew.Chem.,2019,vol.132,p.1145-1149,5

Literature

Title: Didymosphaeria igniaria: a new microorganism useful for the enantioselective reduction of aryl-aliphatic ketones.

Journal: Journal of industrial microbiology & biotechnology 20101101

Title: Synthesis and application of mono-6-(3-methylimidazolium)-6-deoxyperphenylcarbamoyl-beta-cyclodextrin chloride as chiral stationary phases for high-performance liquid chromatography and supercritical fluid chromatography.

Journal: Journal of chromatography. A 20080222

Title: Chiral discrimination in host-guest supramolecular complexes. Understanding enantioselectivity and solid solution behaviors by using spectroscopic methods and chemical sensors.

Journal: The journal of physical chemistry. B 20070628

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