Home Aldehydes 1194-98-5
1194-98-5,MFCD00003333
Catalog No.:AA000IMG

1194-98-5 | 2,5-Dihydroxybenzaldehyde

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250mg
98%
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$6.00   $4.00
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1g
98%
in stock  
$7.00   $5.00
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5g
98%
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$15.00   $11.00
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10g
98%
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$27.00   $19.00
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25g
98%
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$57.00   $40.00
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100g
98%
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$175.00   $123.00
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500g
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$809.00   $567.00
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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:
AA000IMG
Chemical Name:
2,5-Dihydroxybenzaldehyde
CAS Number:
1194-98-5
Molecular Formula:
C7H6O3
Molecular Weight:
138.1207
MDL Number:
MFCD00003333
SMILES:
O=Cc1cc(O)ccc1O
NSC Number:
72387
Properties
Properties
 
BP:
276.1 °C at 760 mmHg  
Form:
Solid  
MP:
97-99 °C  
Refractive Index:
1.4797 (estimate)  
Solubility:
13.8g/l soluble  
Stability:
Air Sensitive  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
124  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
1.2  

Upstream Synthesis Route

[1]ChemicalandPharmaceuticalBulletin,2012,vol.60,#8,p.1046-1054

[1]JournalofMedicinalChemistry,1996,vol.39,#21,p.4261-4274

[1]Tetrahedron,2017,vol.73,#45,p.6393-6400

[2]JournalofOrganicChemistry,2016,vol.81,#22,p.10922-10929

[3]ChemicalCommunications,2012,vol.48,#97,p.11904-11906

[4]EuropeanJournalofOrganicChemistry,2018,vol.2018,#40,p.5605-5614

[5]AppliedOrganometallicChemistry,2015,vol.29,#5,p.322-327

Downstream Synthesis Route

[1]Klein,Emmanuel;DeBonis,Salvatore;Thiede,Bernd;Skoufias,DimitriosA.;Kozielski,Frank;Lebeau,Luc[BioorganicandMedicinalChemistry,2007,vol.15,#19,p.6474-6488]

[2]Salomé,Christophe;Ribeiro,Nigel;Chavagnan,Thierry;Thuaud,Frédéric;Serova,Maria;DeGramont,Armand;Faivre,Sandrine;Raymond,Eric;Désaubry,Laurent[EuropeanJournalofMedicinalChemistry,2014,vol.81,p.181-191]

[3]Neuberger[BiochemicalJournal,1948,vol.43,p.599,602]

[4]Lambooy[JournaloftheAmericanChemicalSociety,1949,vol.71,p.3758]

[5]Takeuchi,Yasuo;Ueda,Norihiro;Uesugi,Koji;Abe,Hitoshi;Nishioka,Hiromi;Harayama,Takashi[Heterocycles,2003,vol.59,#1,p.217-224]

[6]CurrentPatentAssignee:HOSPITALFORSICKCHILDREN(THE)-US2006/58297,2006,A1Locationinpatent:Page/Pagecolumn8

[1]Chemicalandpharmaceuticalbulletin,1978,vol.26,p.191-198

[1]JournalofMedicinalChemistry,1993,vol.36,p.4094-4098

[1]Sharma,RajeshKumar;Priyanka;Katiyar,Diksha[MonatsheftefurChemie,2016,vol.147,#12,p.2157-2161]

[2]Perrella;Chen;Behrens;KaltenbachIII;Seitz[JournalofMedicinalChemistry,1994,vol.37,#14,p.2232-2237]

[1]Cerqueira,NunoM.F.S.A.;Oliveira-Campos,AnaM.F.;Coelho,PauloJ.;MeloDeCarvalho,LuisH.;Samat,Andre;Guglielmetti,Robert[HelveticaChimicaActa,2002,vol.85,#2,p.442-450]

[2]Harayama,Takashi;Katsuno,Keiko;Nishioka,Hiromi;Fujii,Masako;Nishita,Yoshitaka;etal.[Heterocycles,1994,vol.39,#2,p.613-622]

[3]VonWeymarn;Murphy[ChemicalResearchinToxicology,2001,vol.14,#10,p.1386-1392]

Literature

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Journal: International journal of biological macromolecules 20121201

Title: Diffusion-free mediator based miniature biofuel cell anode fabricated on a carbon-MEMS electrode.

Journal: Langmuir : the ACS journal of surfaces and colloids 20121002

Title: Sequential C-N and C-O bond formation in a single pot: synthesis of 2H-benzo[b][1,4]oxazines from 2,5-dihydroxybenzaldehyde and amino acid precursors.

Journal: Organic letters 20120120

Title: Interference of H-bonding and substituent effects in nitro- and hydroxy-substituted salicylaldehydes.

Journal: Journal of molecular modeling 20120101

Title: Synthesis and biological evaluation of phenanthrenes as cytotoxic agents with pharmacophore modeling and ChemGPS-NP prediction as topo II inhibitors.

Journal: PloS one 20120101

Title: Enhanced activity of antifungal drugs using natural phenolics against yeast strains of Candida and Cryptococcus.

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Tags:1194-98-5 Molecular Formula|1194-98-5 MDL|1194-98-5 SMILES|1194-98-5 2,5-Dihydroxybenzaldehyde |Organic_Building_Blocks