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Home Amines 37585-25-4
37585-25-4,MFCD00075163
Catalog No.:AA003GE1

37585-25-4 | 2-Amino-5-chlorobenzyl alcohol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$7.00   $5.00
- +
5g
97%
in stock  
$14.00   $10.00
- +
10g
97%
in stock  
$26.00   $18.00
- +
100g
97%
in stock  
$203.00   $142.00
- +
  • 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:
AA003GE1
Chemical Name:
2-Amino-5-chlorobenzyl alcohol
CAS Number:
37585-25-4
Molecular Formula:
C7H8ClNO
Molecular Weight:
157.5975
MDL Number:
MFCD00075163
SMILES:
OCc1cc(Cl)ccc1N
Properties
Properties
 
Form:
Solid  
MP:
107-109°C(lit.)  
Storage:
Room Temperature;  

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:
1.1  

Upstream Synthesis Route

[1]Patent:WO2010/37533,2010,A1,.Locationinpatent:Page/Pagecolumn45

[2]OrganicProcessResearchandDevelopment,2015,vol.19,#11,p.1548-1553

[3]JournaloftheAmericanChemicalSociety,2013,vol.135,#42,p.15742-15745

[4]AngewandteChemie-InternationalEdition,2017,vol.56,#35,p.10573-10576

[5]Angew.Chem.,2017,vol.129,#35,p.10709-10712,4

[6]Synlett,2017,vol.28,#14,p.1724-1728

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

[8]BioorganicandMedicinalChemistry,2012,vol.20,#19,p.5810-5831

[9]Patent:US2002/103141,2002,A1,

[10]Patent:US6034256,2000,A,

[11]Patent:US6077850,2000,A,

[12]ChemicalCommunications,2016,vol.52,#33,p.5761-5764

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

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

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

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

[4]Patent:WO2010/37533,2010,A1,.Locationinpatent:Page/Pagecolumn44

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

[6]TetrahedronLetters,1995,vol.36,#41,p.7527-7530

[7]Patent:US4164407,1979,A,

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

[9]TetrahedronLetters,2011,vol.52,#45,p.5913-5917

[10]BioorganicandMedicinalChemistry,2012,vol.20,#19,p.5810-5831

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

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

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

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

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

[16]TetrahedronLetters,2017,vol.58,#45,p.4264-4268

[17]OrganicLetters,2018,vol.20,#6,p.1526-1529

[18]OrganicandBiomolecularChemistry,2018,vol.16,#12,p.2039-2042

[1]AngewandteChemie-InternationalEdition,2017,vol.56,#35,p.10573-10576

[2]Angew.Chem.,2017,vol.129,#35,p.10709-10712,4

[3]Synlett,2017,vol.28,#14,p.1724-1728

[1]AngewandteChemie-InternationalEdition,2017,vol.56,#35,p.10573-10576

[2]Angew.Chem.,2017,vol.129,#35,p.10709-10712,4

[3]Synlett,2017,vol.28,#14,p.1724-1728

Downstream Synthesis Route

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

[2]OrganicLetters,2017,vol.19,p.3219-3222

[3]TetrahedronLetters,2017,vol.58,p.3795-3799

[4]Patent:CN108997438,2018,A.Locationinpatent:Paragraph0045;0046;0047

[5]Patent:WO2010/37533,2010,A1.Locationinpatent:Page/Pagecolumn44

[6]Patent:CN110746464,2020,A.Locationinpatent:Paragraph0061-0063

[7]OrganicLetters,2016,vol.18,p.5572-5575

[8]OrganicLetters,2019,vol.21,p.4703-4708

[9]TetrahedronLetters,1995,vol.36,p.7527-7530

[10]Patent:US4164407,1979,A

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

[12]TetrahedronLetters,2011,vol.52,p.5913-5917

[13]BioorganicandMedicinalChemistry,2012,vol.20,p.5810-5831

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

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

[16]OrganicandBiomolecularChemistry,2017,vol.15,p.6474-6477

[17]TetrahedronLetters,2017,vol.58,p.4264-4268

[18]OrganicLetters,2018,vol.20,p.1526-1529

[19]OrganicandBiomolecularChemistry,2018,vol.16,p.2039-2042

[20]TetrahedronLetters,2019,vol.60,p.1967-1970

[1]JournalofMedicinalChemistry,2005,vol.48,p.2080-2092

[2]Patent:US2004/58920,2004,A1.Locationinpatent:Page/Pagecolumn18

[3]Patent:WO2005/14589,2005,A1.Locationinpatent:Page/Pagecolumn168-169

[4]Patent:WO2005/14000,2005,A1.Locationinpatent:Page/Pagecolumn281;329-330

[1]OrganicLetters,2019,vol.21,p.4703-4708

[2]OrganicLetters,2006,vol.8,p.2257-2260

[3]Tetrahedron,2011,vol.67,p.1501-1505

[4]TetrahedronLetters,2010,vol.51,p.5124-5126

[5]ACSCatalysis,2013,vol.3,p.622-624

[6]OrganicandBiomolecularChemistry,2014,vol.12,p.4290-4294

[7]Tetrahedron,2014,vol.70,p.5114-5121

[8]Tetrahedron,2017,vol.73,p.1904-1910

[9]TetrahedronLetters,2017,vol.58,p.3795-3799

[10]TetrahedronLetters,2017,vol.58,p.4264-4268

[11]OrganicLetters,2018,vol.20,p.1473-1476

[12]ChemicalCommunications,2019,vol.55,p.4479-4482

[13]OrganicLetters,2019

[14]TetrahedronLetters,2019,vol.60,p.1967-1970

[15]ChemicalCommunications,2020,vol.56,p.4832-4835

[1]EuropeanJournalofPharmacology,2006,vol.536,p.262-268

[2]Patent:WO2006/21882,2006,A1.Locationinpatent:Page/Pagecolumn29

[1]Patent:WO2010/37533,2010,A1.Locationinpatent:Page/Pagecolumn45

[2]OrganicProcessResearchandDevelopment,2015,vol.19,p.1548-1553

[3]JournaloftheAmericanChemicalSociety,2013,vol.135,p.15742-15745

[4]AngewandteChemie-InternationalEdition,2017,vol.56,p.10573-10576    Angew.Chem.,2017,vol.129,p.10709-10712,4

[5]Synlett,2017,vol.28,p.1724-1728

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

[7]BioorganicandMedicinalChemistry,2012,vol.20,p.5810-5831

[8]Patent:US2002/103141,2002,A1

[9]Patent:US6034256,2000,A

[10]Patent:US6077850,2000,A

[11]ChemicalCommunications,2016,vol.52,p.5761-5764

[12]OrganicandBiomolecularChemistry,2017,vol.15,p.6474-6477

Literature
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SDS
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