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Home Other Building Blocks 526-18-1
526-18-1,MFCD00020026
Catalog No.:AA00DDSG

526-18-1 | Osalmid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25mg
98%
in stock  
$6.00   $4.00
- +
1g
98%
in stock  
$8.00   $6.00
- +
5g
98%
in stock  
$11.00   $8.00
- +
25g
98%
in stock  
$27.00   $19.00
- +
100g
98%
in stock  
$93.00   $65.00
- +
500g
98%
in stock  
$412.00   $288.00
- +
  • 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:
AA00DDSG
Chemical Name:
Osalmid
CAS Number:
526-18-1
Molecular Formula:
C13H11NO3
Molecular Weight:
229.2313
MDL Number:
MFCD00020026
SMILES:
Oc1ccc(cc1)NC(=O)c1ccccc1O
NSC Number:
93960
Properties
Properties
 
BP:
350.8°C at 760 mmHg  
Form:
Solid  
MP:
179°  
Refractive Index:
1.5500 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
261  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
2  
XLogP3:
2.9  

Upstream Synthesis Route

[1]Patent:CN105503633,2016,A,.Locationinpatent:Paragraph0006;0014;0015

[1]BioorganicandMedicinalChemistry,2007,vol.15,#12,p.4113-4124

[1]JournalfuerPraktischeChemie(Leipzig),1900,vol.<2>61,p.552

[2]Chem.Zentralbl.,1900,vol.71,#II,p.612

[3]JournaloftheAmericanChemicalSociety,1947,vol.69,p.2913

[4]Org.Synth.Coll.Vol.III<1955>765,

[5]J.TextileInst.,1930,vol.21,p.245T,255T

[6]JournalfuerPraktischeChemie(Leipzig),1900,vol.<2>61,p.552

[7]Chem.Zentralbl.,1900,vol.71,#II,p.612

[8]JournaloftheAmericanChemicalSociety,1947,vol.69,p.2913

[9]Org.Synth.Coll.Vol.III<1955>765,

[1]JournalofOrganicChemistry,1948,vol.13,p.796,799

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1948,vol.13,p.796,799

[1]JournalfurpraktischeChemie(Leipzig1954),1900,vol.<2>61,p.552    ChemischesZentralblatt,1900,vol.71,p.612

[2]JournaloftheAmericanChemicalSociety,1947,vol.69,p.2913

[3],1930,vol.21,p.245T,255T

[4]JournalfurpraktischeChemie(Leipzig1954),1900,vol.<2>61,p.552    ChemischesZentralblatt,1900,vol.71,p.612

[5]JournaloftheAmericanChemicalSociety,1947,vol.69,p.2913

526-18-1    75-36-5   
1-acetoxy-4-salicyloylamino-benzene 

[1]JournalofOrganicChemistry,1948,vol.13,p.796,799

[1]JournalofOrganicChemistry,1948,vol.13,p.796,799

[1]EuropeanJournalofMedicinalChemistry,1974,vol.9,p.44-50

Literature

Title: Salicylanilides: selective inhibitors of interleukin-12p40 production.

Journal: Bioorganic & medicinal chemistry 20080915

Title: Synthesis, antimicrobial, and QSAR studies of substituted benzamides.

Journal: Bioorganic & medicinal chemistry 20070615

Title: Liu X, et al. Inhibition of hepatitis B virus replication by targeting ribonucleotide reductase M2 protein. Biochem Pharmacol. 2016 Mar 1;103:118-28.

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SDS
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