Skip to Content
Merck
All Photos(1)

Key Documents

138053

Sigma-Aldrich

1-Adamantanecarbonitrile

97%

Synonym(s):

1-Cyanoadamantane

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C11H15N
CAS Number:
Molecular Weight:
161.24
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

193-196 °C (lit.)

SMILES string

N#CC12CC3CC(CC(C3)C1)C2

InChI

1S/C11H15N/c12-7-11-4-8-1-9(5-11)3-10(2-8)6-11/h8-10H,1-6H2/t8-,9+,10-,11-

InChI key

FQFZASRJFRAEIH-BIBSGERRSA-N

General description

1-Adamantanecarbonitrile reacts with W2(OCMe3)6 to yield W(CAd)(OCMe3)3 (Ad=1-adamantyl).

Application

1-Adamantanecarbonitrile was used as starting reagent for the synthesis of adamantyl-l,3,4-oxathiazol-2-one.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

The selective complexation of adamantane nitriles by tungsten pentacarbonyl.
Jefford VJ, et al.
Canadian Journal of Chemistry, 74(1), 107-113 (1996)
α-Hydrogen migration reactions in tungsten (VI) cyclopentadienyl alkylidyne complexes.
Warren TH, et al.
Journal of Organometallic Chemistry, 569(1), 125-137 (1998)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service