69-72-7,MFCD00002439
Catalog No.:AA00FTEJ

69-72-7 | Salicylic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25g
98%
in stock  
$8.00   $6.00
- +
500g
98%
in stock  
$13.00   $9.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00FTEJ
Chemical Name:
Salicylic acid
CAS Number:
69-72-7
Molecular Formula:
C7H6O3
Molecular Weight:
138.1207
MDL Number:
MFCD00002439
SMILES:
C1=CC=C(C(=C1)C(=O)O)O
NSC Number:
180
FEMA Number:
3985
Properties
Properties
 
BP:
211°C at 760 mmHg  
Form:
Solid  
MP:
158-161 °C(lit.)  
Refractive Index:
1,565  
Solubility:
ethanol: 1 M at 20 °C, clear, colorless  
Stability:
Light Sensitive  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
133  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.3  

Upstream Synthesis Route

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

Downstream Synthesis Route
2-ethoxycarbonyloxy-benzoicacid-anhydride 
  2037-95-8    69-72-7 

[1]ChemischeBerichte,1910,vol.43,p.334

4-hydroxy-benzoicacid;sodium-compound 
  636-46-4    609-98-3    69-72-7 

[1]JournalfurpraktischeChemie(Leipzig1954),1877,vol.<2>16,p.442

[1]Patent:DE234217,    Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.10,p.1118

[1]ChemischeBerichte,1902,vol.35,p.3653

[1]JournaloftheAmericanChemicalSociety,1951,vol.73,p.2723

Literature

Title: Mitchell JA, et al. Sodium salicylate inhibits cyclo-oxygenase-2 activity independently of transcription factor (nuclear factor kappaB) activation: role of arachidonic acid. Mol Pharmacol. 1997 Jun;51(6):907-12.

Title: Nixon M, et al. Salicylate downregulates 11β-HSD1 expression in adipose tissue in obese mice and in humans, mediating insulin sensitization. Diabetes. 2012 Apr;61(4):790-6.

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SDS
Tags:69-72-7 Molecular Formula|69-72-7 MDL|69-72-7 SMILES|69-72-7 Salicylic acid
Catalog No.: AA00FTEJ
69-72-7,MFCD00002439
69-72-7 | Salicylic acid
Pack Size: 25g
Purity: 98%
in stock
$8.00 $6.00
Pack Size: 500g
Purity: 98%
in stock
$13.00 $9.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA00FTEJ
Chemical Name: Salicylic acid
CAS Number: 69-72-7
Molecular Formula: C7H6O3
Molecular Weight: 138.1207
MDL Number: MFCD00002439
SMILES: C1=CC=C(C(=C1)C(=O)O)O
NSC Number: 180
FEMA Number: 3985
Properties
BP: 211°C at 760 mmHg  
Form: Solid  
MP: 158-161 °C(lit.)  
Refractive Index: 1,565  
Solubility: ethanol: 1 M at 20 °C, clear, colorless  
Stability: Light Sensitive  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 133  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.3  
Upstream Synthesis Route
76809-28-4    3430-33-9    69-72-7 

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

76809-21-7    1824-81-3    69-72-7 

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

76809-23-9    695-34-1    69-72-7 

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

76809-27-3    3430-27-1    69-72-7 

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

76809-24-0    3430-10-2    69-72-7 

[1]ChemicalandPharmaceuticalBulletin,1980,vol.28,#10,p.3020-3028

Downstream Synthesis Route
2-ethoxycarbonyloxy-benzoicacid-anhydride 
  2037-95-8    69-72-7 

[1]ChemischeBerichte,1910,vol.43,p.334

4-hydroxy-benzoicacid;sodium-compound 
  636-46-4    609-98-3    69-72-7 

[1]JournalfurpraktischeChemie(Leipzig1954),1877,vol.<2>16,p.442

1466-82-6    121-69-7    69-72-7    530-75-6 

[1]Patent:DE234217,    Fortschr.Teerfarbenfabr.Verw.Industriezweige,vol.10,p.1118

57-13-6    69-72-7    2037-95-8    108-80-5 

[1]ChemischeBerichte,1902,vol.35,p.3653

56-23-5    507-40-4    69-72-7    1829-32-9 

[1]JournaloftheAmericanChemicalSociety,1951,vol.73,p.2723

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