Home Other Heterocycles 124-76-5
124-76-5,MFCD00074821
Catalog No.:AA000LBB

124-76-5 | Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R,2R,4R)-rel-

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5g
90%
in stock  
$6.00   $4.00
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25g
90%
in stock  
$8.00   $6.00
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500g
>90.0%(GC)
in stock  
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA000LBB
Chemical Name:
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R,2R,4R)-rel-
CAS Number:
124-76-5
Molecular Formula:
C10H18O
Molecular Weight:
154.2493
MDL Number:
MFCD00074821
SMILES:
O[C@@H]1C[C@@H]2C([C@@]1(C)CC2)(C)C
UN Number:
1312
Properties
Properties
 
BP:
212°C at 760 mmHg  
Form:
Solid  
MP:
212-214 °C (subl.)(lit.)  
Refractive Index:
1.4710 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
185  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
XLogP3:
2.7  

Downstream Synthesis Route

[1]JustusLiebigsAnnalenderChemie,1941,vol.549,p.186,206    ChemischeBerichte,1944,vol.77/79,p.805,808

[1]AnnalesdeChimie(Cachan,France),1878,vol.<5>14,p.11

124-76-5    124-83-4   
(1<i>R</i>)-<i>cis</i>-camphoricaciddi-((1<i>R</i>)-isobornylester) 

[1]JournaloftheAmericanChemicalSociety,1952,vol.74,p.3944

[1]AnnalesdeChimie(Cachan,France),1878,vol.&lt;5&gt;14,p.39

[1]NipponKagakuZasshi,1959,vol.80,p.1366    Chem.Abstr.,1961,p.3644

Literature

Title: Tian LL, Zhou Z, Zhang Q, et al. Protective effect of (+/-) isoborneol against 6-OHDA-induced apoptosis in SH-SY5Y cells. Cell Physiol Biochem. 2007;20(6):1019‐1032.

Title: Armaka M, Papanikolaou E, Sivropoulou A, Arsenakis M. Antiviral properties of isoborneol, a potent inhibitor of herpes simplex virus type 1. Antiviral Res. 1999;43(2):79‐92.

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SDS
Tags:124-76-5 Molecular Formula|124-76-5 MDL|124-76-5 SMILES|124-76-5 Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R,2R,4R)-rel- |Organic_Building_Blocks