Home Amines 20712-12-3
20712-12-3,MFCD08234509
Catalog No.:AA002ISO

20712-12-3 | (2-Amino-5-bromophenyl)methanol

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250mg
98%
in stock  
$7.00   $5.00
- +
1g
98%
in stock  
$12.00   $8.00
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5g
95%
in stock  
$30.00   $21.00
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10g
95%
in stock  
$52.00   $36.00
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25g
95%
in stock  
$119.00   $83.00
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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:
AA002ISO
Chemical Name:
(2-Amino-5-bromophenyl)methanol
CAS Number:
20712-12-3
Molecular Formula:
C7H8BrNO
Molecular Weight:
202.0485
MDL Number:
MFCD08234509
SMILES:
OCc1cc(Br)ccc1N
Properties
Computed Properties
 
Complexity:
110  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
1.4  

Upstream Synthesis Route

[1]OrganicSyntheses,2013,vol.90,p.240-250

[2]ChemistryOpen,2015,vol.4,#2,p.107-110

[3]Patent:CN107304201,2017,A,.Locationinpatent:Paragraph0061;0065

[4]Patent:US6166006,2000,A,

[5]JournalofOrganicChemistry,2010,vol.75,#4,p.1188-1196

[6]Chemistry-AEuropeanJournal,2012,vol.18,#18,p.5530-5535

[7]Patent:WO2014/11900,2014,A2,.Locationinpatent:Page/Pagecolumn37;38

[8]Patent:US2015/197519,2015,A1,.Locationinpatent:Paragraph0127;0128

[9]AdvancedSynthesisandCatalysis,2017,vol.359,#13,p.2191-2195

[10]Patent:US9695165,2017,B2,.Locationinpatent:Page/Pagecolumn38

[11]OrganicandBiomolecularChemistry,2017,vol.15,#31,p.6474-6477

[1]ACSCatalysis,2013,vol.3,#4,p.622-624

[2]ChemicalCommunications,2017,vol.53,#1,p.216-219

[3]OrganicLetters,2017,vol.19,#12,p.3219-3222

[4]Patent:CN107304201,2017,A,.Locationinpatent:Paragraph0061;0064

[5]TetrahedronLetters,2017,vol.58,#40,p.3795-3799

[6]JournalofMedicinalChemistry,2018,

[7]JournalofMedicinalChemistry,2010,vol.53,#17,p.6506-6510

[8]OrganicLetters,2016,vol.18,#9,p.2200-2203

[9]Synlett,2011,#6,p.844-848

[10]JournalofOrganicChemistry,2008,vol.73,#11,p.4252-4255

[11]Chemistry-AEuropeanJournal,2012,vol.18,#18,p.5530-5535

[12]Patent:WO2014/11900,2014,A2,.Locationinpatent:Page/Pagecolumn37

[13]OrganicSyntheses,2013,vol.90,p.240-250

[14]Tetrahedron,2014,vol.70,#34,p.5114-5121

[15]Tetrahedron,2014,vol.70,#34,p.5114-5121

[16]Synthesis(Germany),2014,vol.46,#24,p.3365-3373

[17]Patent:US2015/197519,2015,A1,.Locationinpatent:Paragraph0125;0216

[18]OrganicLetters,2015,vol.17,#19,p.4750-4753

[19]AdvancedSynthesisandCatalysis,2017,vol.359,#13,p.2191-2195

[20]Patent:US9695165,2017,B2,.Locationinpatent:Page/Pagecolumn37;38

[21]OrganicandBiomolecularChemistry,2017,vol.15,#31,p.6474-6477

[1]TetrahedronLetters,2002,vol.43,#7,p.1171-1174

[2]JournalofOrganicChemistry,2014,vol.79,#3,p.1235-1246

[3]Patent:WO2007/115408,2007,A1,.Locationinpatent:Page/Pagecolumn136

[4]OrganicLetters,2016,vol.18,#21,p.5572-5575

[5]Patent:US2011/112067,2011,A1,.Locationinpatent:Page/Pagecolumn33;34

[6]Patent:WO2009/135651,2009,A1,.Locationinpatent:Page/Pagecolumn51

[7]Patent:WO2006/50940,2006,A1,.Locationinpatent:Page/Pagecolumn59-60

[8]Patent:WO2009/7749,2009,A2,.Locationinpatent:Page/Pagecolumn108

[9]JournalofOrganicChemistry,2010,vol.75,#4,p.1188-1196

[10]OrganicLetters,2010,vol.12,#5,p.1084-1087

[11]Patent:WO2006/50943,2006,A1,.Locationinpatent:Page/Pagecolumn45

[12]Patent:WO2011/19090,2011,A1,.Locationinpatent:Page/Pagecolumn47-48

[13]EuropeanJournalofMedicinalChemistry,2014,vol.90,p.788-796

[1]TetrahedronLetters,1996,vol.37,#39,p.6965-6968

[2]Patent:CN105732587,2016,A,.Locationinpatent:Paragraph0111;0112;0113

[3]Patent:CN104650038,2018,B,.Locationinpatent:Paragraph0123;0124;0125

[1]Patent:US6166006,2000,A,

Downstream Synthesis Route

[1]Organicletters,2001,vol.3,p.4217-4220

[1]Patent:WO2007/115408,2007,A1.Locationinpatent:Page/Pagecolumn136

[2]OrganicLetters,2015,vol.17,p.4750-4753

20712-12-3   
(3aS*,4S*,9bS*)-4-(3-aminopropyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo3,2-cquinoline-8-carboxylicacidmethylester 

[1]Organicletters,2001,vol.3,p.4217-4220

[2]Organicletters,2001,vol.3,p.4217-4220

[1]Organicletters,2001,vol.3,p.4217-4220

20712-12-3   
10-bromo-1,2,3,3a,3b,4,5,11b-octahydro-1-(phenylmethyl)-6H-dipyrrolo1,2-a:3',2'-cquinolin-6-one 

[1]Organicletters,2001,vol.3,p.4217-4220

Literature
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SDS
Tags:20712-12-3 Molecular Formula|20712-12-3 MDL|20712-12-3 SMILES|20712-12-3 (2-Amino-5-bromophenyl)methanol