Home Bromides 77337-82-7
77337-82-7,MFCD00041250
Catalog No.:AA003GNH

77337-82-7 | 2-Bromo-5-nitroanisole

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1g
98%
in stock  
$6.00   $4.00
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5g
98%
in stock  
$11.00   $8.00
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25g
96%
in stock  
$45.00   $32.00
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100g
98%
in stock  
$94.00   $66.00
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500g
96%
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$461.00   $323.00
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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:
AA003GNH
Chemical Name:
2-Bromo-5-nitroanisole
CAS Number:
77337-82-7
Molecular Formula:
C7H6BrNO3
Molecular Weight:
232.0314
MDL Number:
MFCD00041250
SMILES:
COc1cc(ccc1Br)[N+](=O)[O-]
NSC Number:
405572
Properties
Properties
 
Form:
Solid  
MP:
99-103 °C  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
171  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
1  
XLogP3:
2.8  

Upstream Synthesis Route

[1]Tetrahedron,2013,vol.69,#16,p.3511-3517

[2]Tetrahedron,2010,vol.66,#37,p.7418-7422

[3]TetrahedronLetters,2010,vol.51,#51,p.6769-6771

[4]ChemicalandPharmaceuticalBulletin,2014,vol.62,#10,p.979-988

[5]JournaloftheAmericanChemicalSociety,1935,vol.57,p.1592,1594

[1]Patent:WO2015/6100,2015,A1,.Locationinpatent:Page/Pagecolumn193;194

[2]JournalofScientificandIndustrialResearch,1954,vol.13B,p.270,271

[1]JournaloftheAmericanChemicalSociety,2012,vol.134,#2,p.1104-1114

[2]LiebigsAnnalenderChemie,1988,p.203-208

[1]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1981,p.2456-2463

[1]JournalofOrganicChemistry,1964,vol.29,p.2605-2609

Downstream Synthesis Route

[1]Patent:WO2015/6100,2015,A1.Locationinpatent:Page/Pagecolumn193;194

[2]JournalOfScientificandIndustrialResearch,1954,vol.13B,p.270,271

[1]Patent:CN109320403,2019,A.Locationinpatent:Paragraph0011;0012;0016;0017

[2]Tetrahedron,2013,vol.69,p.3511-3517

[3]Tetrahedron,2010,vol.66,p.7418-7422

[4]TetrahedronLetters,2010,vol.51,p.6769-6771

[5]ChemicalandPharmaceuticalBulletin,2014,vol.62,p.979-988

[6]JournaloftheAmericanChemicalSociety,1935,vol.57,p.1592,1594

[1]JournaloftheChemicalSociety.PerkintransactionsI,1981,p.2456-2463

[1]Patent:US10000452,2018,B1.Locationinpatent:Page/Pagecolumn117

[2]Patent:US2016/251376,2016,A1.Locationinpatent:Paragraph0539;0540;0541

[3]Patent:WO2008/90353,2008,A1.Locationinpatent:Page/Pagecolumn61

[4]Patent:WO2009/136191,2009,A1.Locationinpatent:Page/Pagecolumn63;64

[5]Patent:WO2012/15723,2012,A1.Locationinpatent:Page/Pagecolumn79;80

[6]JournalofMedicinalChemistry,2011,vol.54,p.8321-8327

[7]Patent:US2013/123258,2013,A1.Locationinpatent:Paragraph0226;0227;0228

[8]Patent:WO2011/119704,2011,A1.Locationinpatent:Page/Pagecolumn47

[9]Tetrahedron,1993,vol.49,p.3053-3064

[10]Patent:US2003/96826,2003,A1

[11]JournalofMedicinalChemistry,2016,vol.59,p.6943-6960

[1]JournaloftheAmericanChemicalSociety,2012,vol.134,p.1104-1114

[2]LiebigsAnnalenderChemie,1988,p.203-208

Literature
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SDS
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