188115
1-Adamantaneethanol
98%
Synonym(s):
2-(1-Adamantyl)ethanol
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About This Item
Empirical Formula (Hill Notation):
C12H20O
CAS Number:
Molecular Weight:
180.29
Beilstein:
1855382
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
mp
66-69 °C (lit.)
functional group
hydroxyl
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
Regulatory Information
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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)
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
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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