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Sigma-Aldrich

(R)-(−)-2-Hexanol

99%

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About This Item

Linear Formula:
CH3(CH2)3CH(OH)CH3
CAS Number:
Molecular Weight:
102.17
Beilstein/REAXYS Number:
1718998
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:

assay

99%

optical activity

[α]24/D −11°, neat

refractive index

n20/D 1.414 (lit.)

bp

137-138 °C (lit.)

density

0.814 g/mL at 20 °C (lit.)

SMILES string

CCCC[C@@H](C)O

InChI

1S/C6H14O/c1-3-4-5-6(2)7/h6-7H,3-5H2,1-2H3/t6-/m1/s1

InChI key

QNVRIHYSUZMSGM-ZCFIWIBFSA-N

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Application

Used in the preparation of key intermediates for model studies in the total synthesis of antivirally active glycolipid cycloviracin B1.

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

123.8 °F - closed cup

flash_point_c

51 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Fangyuan Zhou et al.
The ISME journal, 11(12), 2809-2820 (2017-08-12)
Interactions among microbial symbionts have multiple roles in the maintenance of insect-microbe symbiosis. However, signals mediating microbial interactions have been scarcely studied. In the classical model system of bark beetles and fungal associates, fungi increase the fitness of insects. However
Kazumi Kondo et al.
Journal of medicinal chemistry, 45(17), 3805-3808 (2002-08-09)
The synthesis and evaluation of both the (R)- and (S)-enantioisomers about the 5-position on a tetrahydro-1H-1-benzazepine derivative were described. The absolute configuration of the (R,R)-isomer (10) was determined by X-ray crystallographic analysis. After evaluation of both enantiomers (compounds R-2, S-2)

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