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Merck
CN

130346

1-Adamantanol

ReagentPlus®, 99%

Synonym(s):

1-Hydroxyadamantane

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
Molecular Weight:
152.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-202-8
Beilstein/REAXYS Number:
1903952
MDL number:
Assay:
99%
Form:
powder
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Product Name

1-Adamantanol, ReagentPlus®, 99%

InChI key

VLLNJDMHDJRNFK-CHIWXEEVSA-N

InChI

1S/C10H16O/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9,11H,1-6H2/t7-,8+,9-,10-

SMILES string

OC12C[C@H]3C[C@H](C[C@H](C3)C1)C2

product line

ReagentPlus®

assay

99%

form

powder

mp

247 °C (subl.) (lit.)

functional group

hydroxyl

Quality Level

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Application

1-Adamantanol was used in the preparation of 1,3-adamantanediol.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Koichi Mitsukura et al.
Journal of bioscience and bioengineering, 109(6), 550-553 (2010-05-18)
To efficiently produce 1,3-adamantanediol (1,3-ad(OH)(2)) from 1-adamantanol (1-adOH), our stocks of culture strains and soil microorganisms were surveyed for hydroxylation activity towards 1-adOH. Among them, the soil actinomycete SA8 showing the highest hydroxylation activity was identified as Streptomyces sp. based
Motowo Yamaguchi et al.
Inorganic chemistry, 45(20), 8342-8354 (2006-09-27)
New ruthenium(II) complexes having a tetradentate ligand such as tris(2-pyridylmethyl)amine (TPA), tris[2-(5-methoxycarbonyl)pyridylmethyl]amine [5-(MeOCO)3-TPA], tris(2-quinolylmethyl)amine (TQA), or bis(2-pyridylmethyl)glycinate (BPG) have been prepared. The reaction of the ligand with [RuCl2(Me2SO)4] resulted in a mixture of trans and cis isomers of the chloro(dimethyl

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