Home Aldehydes 20028-53-9
20028-53-9,MFCD02093936
Catalog No.:AA002CKJ

20028-53-9 | 2-Amino-5-chlorobenzaldehyde

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250mg
98%
in stock  
$15.00   $11.00
- +
1g
98%
in stock  
$18.00   $13.00
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5g
98%
in stock  
$66.00   $47.00
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10g
98%
in stock  
$124.00   $87.00
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25g
98%
in stock  
$284.00   $199.00
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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:
AA002CKJ
Chemical Name:
2-Amino-5-chlorobenzaldehyde
CAS Number:
20028-53-9
Molecular Formula:
C7H6ClNO
Molecular Weight:
155.5816
MDL Number:
MFCD02093936
SMILES:
O=Cc1cc(Cl)ccc1N
Properties
Computed Properties
 
Complexity:
129  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.3  

Upstream Synthesis Route

[1]ChemicalCommunications,2011,vol.47,#33,p.9513-9515

[1]TetrahedronLetters,2015,vol.56,#7,p.889-892

[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]OrganicLetters,2010,vol.12,#23,p.5502-5505

[2]Patent:US2006/63841,2006,A1,.Locationinpatent:Page/Pagecolumn30;6/12

[3]ChemicalCommunications,2011,vol.47,#36,p.10133-10135

[4]Synthesis(Germany),2016,vol.48,#22,p.3985-3995

[5]Journalofmedicinalchemistry,1968,vol.11,#5,p.946-949

[6]Heterocycles,2005,vol.65,#9,p.2095-2105

[7]OrganicLetters,2008,vol.10,#2,p.173-175

[8]BioorganicandMedicinalChemistry,2009,vol.17,#24,p.8221-8233

[9]OrganicLetters,2010,vol.12,#12,p.2841-2843

[10]ChemicalCommunications,2010,vol.46,#29,p.5244-5246

[11]ChemicalCommunications,2011,vol.47,#33,p.9513-9515

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

[13]ACSCombinatorialScience,2012,vol.14,#5,p.316-322

[14]Patent:US2013/190500,2013,A1,.Locationinpatent:Paragraph0016;0017

[15]Patent:WO2017/35077,2017,A1,.Locationinpatent:Paragraph00192

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

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

[18]BioorganicandMedicinalChemistryLetters,2017,vol.27,#17,p.4128-4132

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

[20]Patent:CN107522766,2017,A,.Locationinpatent:Paragraph0147;0148;0149

[21]Patent:WO2018/39197,2018,A1,.Locationinpatent:Paragraph00194

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

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

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,1993,vol.36,p.2689-2700

[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

[1]Wang,Kan;Herdtweck,Eberhardt;Doemling,Alexander[ACSCombinatorialScience,2012,vol.14,#5,p.316-322]

[1]Locationinpatent:experimentalpartWang,Kan;Herdtweck,Eberhardt;Doemling,Alexander[ACSCombinatorialScience,2012,vol.14,#5,p.316-322]

[1]Wang,Kan;Herdtweck,Eberhardt;Doemling,Alexander[ACSCombinatorialScience,2012,vol.14,#5,p.316-322]

Literature

Title: Virtual screening identification of nonfolate compounds, including a CNS drug, as antiparasitic agents inhibiting pteridine reductase.

Journal: Journal of medicinal chemistry 20110113

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SDS
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