Chemodex

1-Adamantanol

Product Code:
 
CDX-A0811
Product Group:
 
Other Biochemicals
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
Short term: +4°C. Long term: -20°C
Chemical Structure

Chemical Structure 

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CDX-A0811-G02525 g£81.00
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This product comes from: Switzerland.
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  • Further Information
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Further Information

Appearance:
White to off-white powder or crystals.
CAS:
768-95-6
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.
EClass:
32160000
Form:
solid
Handling Advice:
Protect from light and moisture.
InChi:
InChI=1S/C10H16O/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9,11H,1-6H2/t7-,8+,9-,10?
InChi Key:
VLLNJDMHDJRNFK-URIMCQPQSA-N
MDL:
MFCD00074729
Molecular Formula:
C10H16O
Molecular Weight:
152.23
Package Type:
Vial
Purity:
>99% (GC)
SMILES:
OC12C[C@H](C3)C[C@@H](C2)C[C@H]3C1
Solubility:
Soluble in chloroform, methanol or ethanol. Insoluble in water.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

Documents

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)