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Sigma-Aldrich

1-Adamantaneethanol

98%

Synonym(s):

2-(1-Adamantyl)ethanol

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About This Item

Empirical Formula (Hill Notation):
C12H20O
CAS Number:
6240-11-5
Molecular Weight:
180.29
Beilstein/REAXYS Number:
1855382
EC Number:
228-353-8
MDL number:
MFCD00074756
UNSPSC Code:
12352100
PubChem Substance ID:
24851298
NACRES:
NA.22

assay

98%

mp

66-69 °C (lit.)

SMILES string

OCCC12C[C@H]3C[C@H](C[C@H](C3)C1)C2

InChI

1S/C12H20O/c13-2-1-12-6-9-3-10(7-12)5-11(4-9)8-12/h9-11,13H,1-8H2/t9-,10+,11-,12+

InChI key

ZBIDZPHRNBZTLT-BKUVIOGVSA-N

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Application

1-Adamantaneethanol was used in the synthesis of:
  • 4-(adamant-1-ylethylenoxycarbonyl)phthalanhydride
  • poly(2-methoxy-5-cyclohexylmethyloxy-p-phenylene vinylene)
  • adamantine-containing phthalocyanines

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A Orzeszko et al.
Farmaco (Societa chimica italiana : 1989), 55(9-10), 619-623 (2001-01-11)
A series of new derivatives of adamantane was synthesised. The new compound 4-(adamant-1-ylethylenoxycarbonyl)phthalanhydride obtained from 1-adamantaneethanol and trimellitic anhydride chloride, as well as 4-(adamant-1-ylmethylenoxycarbonyl)phthalanhydride, appeared very useful for preparation of a number of N-substituted phthalimides. Antimicrobial activity of newly obtained
Synthesis and characterization of the first adamantane-based poly (p-phenylenevinylene) derivative: an intelligent plastic for smart electronic displays.
Jeong HY, et al.
Thin Solid Films, 417(1), 171-174 (2002)
Highly photostable silicon (IV) phthalocyanines containing adamantane moieties: synthesis, structure, and properties.
Shen X-M, et al.
Tetrahedron, 66(46), 9041-9048 (2010)

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