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287784

(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

UNSPSC Code:

12352001

NACRES:

NA.22

PubChem Substance ID:

24857292

MDL number:

MFCD09955216

Beilstein/REAXYS Number:

2039144

Assay:

99%

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Properties

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.)

functional group

hydroxyl

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

Description

Application

Used to prepare chiral double allylation reagents.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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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

Global Trade Item Number

SKU	GTIN
287784-5G	04061832719030
287784-1G	04061826266366