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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:
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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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