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(1R,2R,3R,5S)-(−)-Isopinocampheol / 25 G

Purity: 98 %
Synonym: 3-Pinanol; (1R,2R,3R,5S)-3-Pinanol; (−)-Isopinocampheol; (1R,2R,3R,5S)-2,6,6-Trimethylbicyclo[3.1.1]heptan-3-ol
Molecular Formula: C10H18O
Molecular Weight: 154.25
SKU: MND-53653
CAS Number: 25465-65-0
MDL number: MFCD00064146
EC Number: 247-011-9
PubChem: 24852964
Form: solid
Packing size: 25 G  
130.90 EUR


Properties

Flash Point (C)93.4 °C - closed cup
Boiling Point219 °C (lit.)
Melting Point51-53 °C (lit.)

 Product Description

(1R,2R,3R,5S)-(−)-Isopinocampheol is a chiral compound with a bicyclic structure. It is commonly used as a chiral auxiliary in asymmetric synthesis and as a building block in organic chemistry.

 

Application:

(1R,2R,3R,5S)-(−)-Isopinocampheol is primarily employed as a chiral auxiliary in asymmetric synthesis to control the stereochemistry of reactions. It also serves as a precursor for the synthesis of various complex molecules in organic chemistry.

 

 

 

Articles:

- Reduction of 2, 3-epoxypinane and 3, 4-epoxyc arane

Publication Date: June 1959

Z. G. Isaeva & B. A. Arbuzov

https://doi.org/10.1007/BF00916669

 

- Proton Transfer Reaction - Mass Spectrometry Determination of the Emission Rate of Flavor Ingredients in Toothpastes

Publication Date: February 2013

Ge Zhang, Sheng Nan Gao, Wen Ding Wei, Qiu Jian Xu

https://doi.org/10.4028/www.scientific.net/AMM.299.229

 

- Zur Kenntnis des Rosenöls. 2. Mitteilung. Die Konstitution des Oxyds C10H18O aus bulgarischem Rosenöl

Publication Date: 1961

C. F. Seidel, Dorothee Felix, A. Eschenmoser, K. Biemann, E. Palluy, M. Stoll

https://doi.org/10.1002/hlca.19610440226