Home Aldehydes 1761-62-2
1761-62-2,MFCD00723501
Catalog No.:AA0021CW

1761-62-2 | 2-hydroxy-5-iodobenzaldehyde

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250mg
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$7.00   $5.00
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1g
98%
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$9.00   $7.00
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5g
98%
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$42.00   $29.00
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10g
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100g
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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:
AA0021CW
Chemical Name:
2-hydroxy-5-iodobenzaldehyde
CAS Number:
1761-62-2
Molecular Formula:
C7H5IO2
Molecular Weight:
248.0179
MDL Number:
MFCD00723501
SMILES:
O=Cc1cc(I)ccc1O
NSC Number:
74697
Properties
Computed Properties
 
Complexity:
127  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2.2  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,2015,vol.80,#9,p.4306-4312

[2]Synlett,2014,vol.25,#3,p.399-402

[3]EuropeanJournalofOrganicChemistry,2016,vol.2016,#12,p.2177-2186

[4]AngewandteChemie-InternationalEdition,2007,vol.46,#4,p.572-575

[5]Chemistry-AEuropeanJournal,2013,vol.19,#7,p.2442-2449

[6]AdvancedSynthesisandCatalysis,2004,vol.346,#1,p.77-82

[7]Patent:CN104059378,2016,B,.Locationinpatent:Paragraph0021-0023

[8]SyntheticCommunications,1999,vol.29,#12,p.2061-2068

[9]EuropeanJournalofOrganicChemistry,2011,#17,p.3137-3145

[10]Chemistry-AEuropeanJournal,2013,vol.19,#17,p.5375-5386

[11]RSCAdvances,2014,vol.4,#12,p.6267-6274

[12]SynthesisandReactivityinInorganic,Metal-OrganicandNano-MetalChemistry,2016,vol.46,#6,p.832-837

[13]AsianJournalofChemistry,2018,vol.30,#8,p.1892-1896

[14]MonatsheftefurChemie,2016,vol.147,#3,p.509-521

[15]Patent:US2007/129288,2007,A1,.Locationinpatent:Page/Pagecolumn23

[16]AppliedOrganometallicChemistry,2013,vol.27,#12,p.695-697

[17]Patent:US8822713,2014,B2,.Locationinpatent:Paragraph8;9

[18]BioorganicandMedicinalChemistry,1996,vol.4,#5,p.659-666

[19]Patent:US6034093,2000,A,

[20]Patent:US5731315,1998,A,

[21]Patent:US2012/217432,2012,A1,

[22]DaltonTransactions,2014,vol.43,#31,p.11897-11907

[23]JournalofPharmacyandPharmacology,2016,vol.68,#2,p.233-244

[1]Patent:WO2004/87686,2004,A2,.Locationinpatent:Page325

[2]Patent:WO2004/87687,2004,A1,.Locationinpatent:Page325

[3]Chemistry-AEuropeanJournal,2018,vol.24,#62,p.16670-16676

[4]TetrahedronLetters,2005,vol.46,#32,p.5285-5287

[5]BioorganicandMedicinalChemistryLetters,2008,vol.18,#20,p.5591-5593

[1]Patent:WO2008/57336,2008,A2,.Locationinpatent:Page/Pagecolumn80

[1]JournalofOrganicChemistry,2006,vol.71,#9,p.3646-3649

[1]Patent:US6034256,2000,A,

[2]Patent:US6077850,2000,A,

Downstream Synthesis Route

[1]SyntheticCommunications,1999,vol.29,p.2061-2068

1761-62-2    137848-29-4   
2'-1-(2-Hydroxy-5-iodo-phenyl)-meth-(E)-ylidene-amino}-1,1'binaphthalenyl-2-ol 

[1]Chemistry-AEuropeanJournal,2002,vol.8,p.5033-5042

[1]SyntheticCommunications,2005,vol.35,p.1851-1857

[1]Tchilibon,Susanna;Joshi,BhalchandraV.;Kim,Soo-Kyung;Duong,HengT.;Gao,Zhan-Guo;Jacobson,KennethA.[JournalofMedicinalChemistry,2005,vol.48,#6,p.1745-1758]

[2]He,Yu-Peng;Tan,Hao;Arve,Lars;Baumann,Sascha;Waldmann,Herbert;Arndt,Hans-Dieter[Chemistry-AnAsianJournal,2011,vol.6,#6,p.1546-1556]

[3]CurrentPatentAssignee:ROCHEHOLDINGAG-WO2014/9495,2014,A1Locationinpatent:Page/Pagecolumn43

[4]CurrentPatentAssignee:GOVERNMENTOFTHEUNITEDSTATES-WO2006/31505,2006,A1Locationinpatent:Page/Pagecolumn28

[1]Trobe,Melanie;Vareka,Martin;Schreiner,Till;Dobrounig,Patrick;Doler,Carina;Holzinger,EllaB.;Steinegger,Andreas;Breinbauer,Rolf[EuropeanJournalofOrganicChemistry,2022,vol.2022,#17]

[2]Locationinpatent:experimentalpartSmith,MarkE.B.;Gunn,RichardM.;Rosivatz,Evelyn;Mak,LokH.;Woscholski,Ruediger;Hailes,HelenC.[BioorganicandMedicinalChemistry,2010,vol.18,#14,p.4917-4927]

[3]Lee,SeungHwan;Nam,MiHye;Cho,MinYoung;Yoo,ByungWoo;Rhee,HakJune;Yoon,CheolMin[SyntheticCommunications,2006,vol.36,#17,p.2469-2474]

Literature

Title: (E)-2-(2-Hy-droxy-5-iodo-benzyl-idene)hydrazinecarboxamide.

Journal: Acta crystallographica. Section E, Structure reports online 20120401

Title: N'-[(E)-2-Hy-droxy-5-iodo-benzyl-idene]furan-2-carbohydrazide monohydrate.

Journal: Acta crystallographica. Section E, Structure reports online 20120201

Title: Synthesis of linear and tripoidal oligo(phenylene ethynylene)-based building blocks for application in modular DNA-programmed assembly.

Journal: The Journal of organic chemistry 20040402

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