Chemodex

1-Adamantanol

As low as CHF 77.00
In stock
Only %1 left
CDX-A0811-G02525 gCHF 77.00
NEW
 
More Information
Product Details
Synonyms 1-Hydroxyadamantan; 1-Adamantyl alcohol; Adamantan-1-ol; NSC 108837
Product Type Chemical
Properties
Formula C10H16O
MW 152.23
CAS 768-95-6
RTECS AU4980000
Source/Host Chemicals Synthetic
Purity Chemicals ≥99% (GC)
Appearance White to off-white powder or crystals.
Solubility Soluble in chloroform, methanol or ethanol. Insoluble in water.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key VLLNJDMHDJRNFK-URIMCQPQSA-N
Smiles OC12C[C@H](C3)C[C@@H](C2)C[C@H]3C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
1-Adamantanol is a compound that functions as a versatile building block in organic synthesis. It serves as a precursor for the preparation of various derivatives, including polymers, and specialty chemicals. Its mechanism of action involves participating in a range of chemical reactions, such as esterification, etherification and oxidation, to yield structurally diverse products. 1-Adamantanol's molecular structure allows it to undergo selective functionalization, enabling the creation of new compounds with tailored properties. Its role in the synthesis of complex molecules may be useful for exploring the structure-activity relationships of organic compounds. At the molecular level, 1-Adamantanol's functional groups facilitate its reactivity, leading to the formation of novel chemical entities with potential applications in various fields of study.
Product References
(1) K. Mitsukura, et al.; J. Biosci. Bioeng. 109, 550 (2010) | (2) A.A. Awasthi, et al.; Chemphyschem. 22, 975 (2021) | (3) J.W. Wang, et al.; Molecules 26, 2412 (2021) | (4) K.L. Mears, et al.; Angew. Chem. Int. Ed. Engl. 61, e202201318 (2022) | (5) F.T. Meng, et al.; Nat. Commun. 13, 7393 (2022) | (6) P. Jesionek, et al.; Spectrochim. Acta A Mol. Biomol. Spectrosc. 299, 122794 (2023)
© 2017 Adipogen Life Sciences. Pictures: © 2012 Martin Oeggerli. All Rights Reserved.