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(1R,2R,3S,5R)-(−)-Pinanediol

Name: (1R,2R,3S,5R)-(−)-Pinanediol
Brand: ALDRICH

99%

Synonym(s):

(−)-2-Hydroxyisopinocampheol, [1R-(1α,2α,3α,5α)]-2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₁₈O₂

CAS Number:

22422-34-0

Molecular Weight:

170.25

Beilstein:

2039144

MDL number:

MFCD09955216

UNSPSC Code:

12352001

PubChem Substance ID:

24857292

NACRES:

NA.22

Quality Level

200

Assay

99%

optical activity

[α]21/D −8.6°, c = 6.5 in toluene

optical purity

ee: 97% (GLC)

bp

101-102 °C/1 mmHg (lit.)

mp

57-59 °C (lit.)

SMILES string

CC1(C)[C@H]2C[C@H](O)[C@](C)(O)[C@@H]1C2

InChI

1S/C10H18O2/c1-9(2)6-4-7(9)10(3,12)8(11)5-6/h6-8,11-12H,4-5H2,1-3H3/t6-,7-,8+,10-/m1/s1

InChI key

MOILFCKRQFQVFS-BDNRQGISSA-N

Related Categories

Chiral Catalysts & Ligands

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Application

Used to prepare chiral double allylation reagents.

WGK

WGK 3

Flash Point(F)

230.0 °F

Flash Point(C)

110 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Simple, stable, and versatile double-allylation reagents for the stereoselective preparation of skeletally diverse compounds.

Feng Peng et al.

Journal of the American Chemical Society, 129(11), 3070-3071 (2007-02-24)

Chiral recognition of amino acids by use of a fluorescent resorcinarene.

Gerald I Richard et al.

Applied spectroscopy, 62(5), 476-480 (2008-05-24)

The spectroscopic properties of a chiral boronic acid based resorcinarene macrocycle employed for chiral analysis were investigated. Specifically, the emission and excitation characteristics of tetraarylboronate resorcinarene macrocycle (TBRM) and its quantum yield were evaluated. The chiral selector TBRM was investigated

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