Home Bromides 6626-15-9
6626-15-9,MFCD00002272
Catalog No.:AA003KYE

6626-15-9 | 4-Bromoresorcinol

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1g
96%
in stock  
$16.00   $11.00
- +
5g
96%
in stock  
$27.00   $19.00
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10g
96%
in stock  
$33.00   $23.00
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25g
96%
in stock  
$75.00   $53.00
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100g
96%
in stock  
$281.00   $197.00
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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:
AA003KYE
Chemical Name:
4-Bromoresorcinol
CAS Number:
6626-15-9
Molecular Formula:
C6H5BrO2
Molecular Weight:
189.0067
MDL Number:
MFCD00002272
SMILES:
Oc1ccc(c(c1)O)Br
NSC Number:
59699
Properties
Properties
 
BP:
302.6 °C at 760 mmHg  
Form:
Solid  
MP:
97-100 °C(lit.);  
Refractive Index:
1.4925 (estimate)  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
97.1  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
XLogP3:
2.2  

Upstream Synthesis Route

[1]SyntheticCommunications,2007,vol.37,#2,p.323-328

[2]Polyhedron,2013,vol.52,p.246-254

[3]SyntheticCommunications,2001,vol.31,#19,p.2955-2963

[4]TetrahedronLetters,2003,vol.44,#9,p.1815-1817

[5]Tetrahedron,2010,vol.66,#34,p.6906-6911

[6]JournaloftheSerbianChemicalSociety,2011,vol.76,#5,p.685-692

[7]OrientalJournalofChemistry,2011,vol.27,#2,p.429-434

[8]MonatsheftefurChemie,2013,vol.144,#2,p.179-181

[9]SyntheticCommunications,2010,vol.40,#21,p.3226-3232

[10]TetrahedronLetters,2007,vol.48,#7,p.1255-1259

[11]TetrahedronLetters,2010,vol.51,#2,p.340-342

[12]Chemistry-AnAsianJournal,2009,vol.4,#8,p.1213-1216

[13]OrganicLetters,2015,vol.17,#4,p.1046-1049

[14]SyntheticCommunications,2009,vol.39,#23,p.4212-4220

[15]ZhurnalObshcheiKhimii,1933,vol.3,p.172,173,174

[16]Chem.Zentralbl.,1934,vol.105,#I,p.1476

[17]ZhurnalObshcheiKhimii,1952,vol.22,p.1594,1597;engl.Ausg.S.1635,1637

[18]JournalofOrganicChemistry,1979,vol.44,p.4733-4735

[19]JournaloftheAmericanChemicalSociety,1988,vol.110,#2,p.546-551

[20]TetrahedronLetters,2008,vol.49,#1,p.189-194

[21]Synthesis,2010,#10,p.1629-1632

[22]TetrahedronLetters,2010,vol.51,#33,p.4415-4418

[23]TetrahedronLetters,2012,vol.53,#2,p.127-131

[24]JournalofMolecularCatalysisA:Chemical,2012,vol.358,p.38-48

[25]CatalysisLetters,2013,vol.143,#2,p.225-233

[26]Synthesis(Germany),2013,vol.45,#11,p.1497-1504

[27]JournalofOrganometallicChemistry,2014,vol.761,p.169-178

[28]JournalofOrganometallicChemistry,2018,vol.858,p.37-46

[1]Tetrahedron,2016,vol.72,#26,p.3653-3665

[1]JournaloftheIndianChemicalSociety,1937,vol.14,p.725,731

[2]MonatsheftefuerChemie,1887,vol.8,p.293

[3]JournaloftheAmericanChemicalSociety,1926,vol.48,p.3127

[4]OrganicSyntheses,1937,vol.17,p.24

[5]Coll.Vol.,1943,vol.II,p.100

[1]CanadianJournalofChemistry,1988,vol.66,p.2431-2439

[1]JournaloftheAmericanChemicalSociety,1926,vol.48,p.3127

[2]OrganicSyntheses,1937,vol.17,p.24

[3]Coll.Vol.,1943,vol.II,p.100

Downstream Synthesis Route

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1980,vol.19,p.129-131

[1]Lichoschersstow[ZhurnalObshcheiKhimii,1933,vol.3,p.172,173,174][ChemischesZentralblatt,1934,vol.105,#I,p.1476]

[1]Zehenter[MonatsheftefurChemie,1887,vol.8,p.293]

[1]JournaloftheAmericanChemicalSociety,2007,vol.129,p.3918-3929

[2]JournaloftheAmericanChemicalSociety,1991,vol.113,p.9293-9319

[1]JournalOfScientificandIndustrialResearch,1952,vol.11B,p.39,43

Literature

Title: Synthesis and antimicrobial activity of brominated resorcinol dimers.

Journal: Bioorganic & medicinal chemistry letters 20111201

Title: Photocatalytic degradation of p-halophenols in TiO2 aqueous suspensions: halogen effect on removal rate, aromatic intermediates and toxicity variations.

Journal: Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering 20060101

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