(1S,2S,3R,5S)-(+)-2,3-Pinanediol

Names

[ Name ]:
(1S,2S,3R,5S)-(+)-2,3-Pinanediol

[Synonym ]:
Bicyclo[3.1.1]heptane-2,3-diol, 2,6,6-trimethyl-, (1R,3R)-
(1S,2S,3R|,5S)-(+)-Pinanediol
(1R,3R)-2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol
(+)-2-Hydroxyisopinocampheol
(1S,2S,3R,5S)-2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol
(1S,2S,3R,5S)-(+)-2,3-Pinanediol
(1S,2S,3R,5S)-(+)-Pinanediol
Pinanediol,(+)
MFCD00077851
UNII-Y6ZCV4AVRA
(1S,2S,3R,5S)-2,6,6-Trimethylbicyclo[3.1.1]heptan-2,3-diol
Bicyclo[3.1.1]heptane-2,3-diol, 2,6,6-trimethyl-, (1S,2S,3R,5S)-
2alpha,3alpha-Pinanediol

Biological Activity

[Description]:

(1S,2S,3R,5S)-(+)-Pinanediol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

[In Vitro]

(+)-Pinanediol 是黑色素生成的有效诱导剂。在 S91 细胞中，它通过诱导更高水平的色素沉着和一氧化氮 (NO) 的合成起作用。

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
263.7±8.0 °C at 760 mmHg

[ Melting Point ]:
53-57ºC

[ Molecular Formula ]:
C₁₀H₁₈O₂

[ Molecular Weight ]:
170.25

[ Flash Point ]:
120.8±13.0 °C

[ Exact Mass ]:
170.130676

[ PSA ]:
40.46000

[ LogP ]:
1.58

[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C

[ Index of Refraction ]:
1.520

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2906199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2906199090

[ Summary ]:
2906199090. cyclanic, cyclenic or cyclotherpenic alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

Enantio- and diastereoselective synthesis of syn-beta-hydroxyallylsilanes via a chiral (Z)-gamma-silylallylboronate.

Org. Lett. 9 , 4315, (2007)

syn-beta-Hydroxyallylsilanes of general structure 11 and 28 are prepared in 50-86% yield and 91-95% ee (for aliphatic aldehydes; 50% ee for benzaldehyde) via the BF(3).Et(2)O-promoted gamma-silylallyl...

J. Org. Chem. 58 , 3600, (1993)

Tetrahedron 49 , 1009, (1993)

Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.