Home Bromides 100751-63-1
100751-63-1,MFCD09842470
Catalog No.:AA0002QG

100751-63-1 | (6-bromonaphthalen-2-yl)methanol

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Purity
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100mg
97%
in stock  
$7.00   $5.00
- +
250mg
97%
in stock  
$13.00   $9.00
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1g
97%
in stock  
$48.00   $34.00
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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:
AA0002QG
Chemical Name:
(6-bromonaphthalen-2-yl)methanol
CAS Number:
100751-63-1
Molecular Formula:
C11H9BrO
Molecular Weight:
237.0926
MDL Number:
MFCD09842470
SMILES:
OCc1ccc2c(c1)ccc(c2)Br
Properties
Computed Properties
 
Complexity:
172  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.9  

Upstream Synthesis Route

[1]Patent:US2006/159953,2006,A1,.Locationinpatent:Page/Pagecolumn4

[2]JournalofOrganometallicChemistry,2013,vol.745-746,p.177-185

[1]BioorganicandMedicinalChemistryLetters,2008,vol.18,#1,p.267-273

[2]Patent:WO2009/130475,2009,A1,.Locationinpatent:Page/Pagecolumn31-32

[3]Patent:WO2016/40891,2016,A2,.Locationinpatent:Paragraph00335

[4]Patent:WO2005/40157,2005,A2,.Locationinpatent:Page/Pagecolumn83

[5]Patent:WO2016/112284,2016,A1,.Locationinpatent:Page/Pagecolumn132;133

[6]JournalofMedicinalChemistry,1993,vol.36,#17,p.2485-2493

[7]Patent:JP2016/37458,2016,A,

[8]Patent:WO2018/118838,2018,A1,.Locationinpatent:Paragraph00249

[9]Patent:CN108530392,2018,A,.Locationinpatent:Paragraph0025;0033;0035

[1]Patent:US2004/92521,2004,A1,.Locationinpatent:Page/Pagecolumn30

[2]Tetrahedron,2009,vol.65,#7,p.1349-1360

[3]OrganicProcessResearchandDevelopment,2007,vol.11,#6,p.1004-1009

[4]BioorganicandMedicinalChemistryLetters,2007,vol.17,#5,p.1443-1446

[5]Patent:WO2008/91130,2008,A1,.Locationinpatent:Page/Pagecolumn11-12

[6]AngewandteChemie-InternationalEdition,2014,vol.53,#13,p.3436-3441

[7]Angew.Chem.,2014,vol.126,#13,p.3504-3509,6

[8]Patent:US2006/159953,2006,A1,.Locationinpatent:Page/Pagecolumn4

[9]BioorganicandMedicinalChemistry,2017,vol.25,#16,p.4355-4367

[10]Patent:WO2013/25733,2013,A1,.Locationinpatent:Paragraph0633

[11]Patent:WO2007/90886,2007,A1,.Locationinpatent:Page/Pagecolumn17

[12]ChemicalandPharmaceuticalBulletin,2000,vol.48,#5,p.694-707

[13]Patent:WO2011/72257,2011,A2,.Locationinpatent:Page/Pagecolumn44-45

[14]JournaloftheAmericanChemicalSociety,2012,vol.134,#42,p.17338-17341,4

[15]JournaloftheAmericanChemicalSociety,2012,vol.134,#42,p.17338-17341

[16]ChemicalCommunications,2015,vol.51,#1,p.125-128

[17]Patent:JP2016/37458,2016,A,.Locationinpatent:Paragraph0172;0174

[1]BioorganicandMedicinalChemistry,2017,vol.25,#16,p.4355-4367

[1]Patent:US2002/143182,2002,A1,

Downstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.267-273

[2]Patent:WO2009/130475,2009,A1.Locationinpatent:Page/Pagecolumn31-32

[3]Patent:WO2016/40891,2016,A2.Locationinpatent:Paragraph00335

[4]Patent:WO2005/40157,2005,A2.Locationinpatent:Page/Pagecolumn83

[5]Patent:WO2016/112284,2016,A1.Locationinpatent:Page/Pagecolumn132;133

[6]BioorganicandMedicinalChemistry,2019,vol.27,p.692-699

[7]JournalofMedicinalChemistry,1993,vol.36,p.2485-2493

[8]Patent:JP2016/37458,2016,A

[9]Patent:WO2018/118838,2018,A1.Locationinpatent:Paragraph00249

[10]Patent:CN108530392,2018,A.Locationinpatent:Paragraph0025;0033;0035

[11]JournalofMaterialsChemistryC,2020,vol.8,p.3165-3175

[1]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.1443-1446

[2]Patent:US2004/92521,2004,A1.Locationinpatent:Page/Pagecolumn30

[3]AngewandteChemie-InternationalEdition,2014,vol.53,p.3436-3441    Angew.Chem.,2014,vol.126,p.3504-3509,6

[4]OrganicProcessResearchandDevelopment,2007,vol.11,p.1004-1009

[5]Patent:WO2013/25733,2013,A1.Locationinpatent:Paragraph0634

[6]Patent:EP3239143,2017,A2.Locationinpatent:Paragraph0309

[7]JournalofMedicinalChemistry,1993,vol.36,p.2485-2493

[1]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.1443-1446

[2]OrganicProcessResearchandDevelopment,2007,vol.11,p.1004-1009

[3]BioorganicandMedicinalChemistry,2017,vol.25,p.4355-4367

[1]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.1443-1446

100751-63-1   
4-{6-2-(dimethylamino)ethyl-2-naphthyl}benzonitrile 

[1]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.1443-1446

Literature
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SDS
Tags:100751-63-1 Molecular Formula|100751-63-1 MDL|100751-63-1 SMILES|100751-63-1 (6-bromonaphthalen-2-yl)methanol