Date published: 2026-1-8

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α-Cyclopropylbenzyl alcohol (CAS 1007-03-0)

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CAS Number:
1007-03-0
Molecular Weight:
148.20
Molecular Formula:
C10H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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α-Cyclopropylbenzyl alcohol is a compound that functions as a chemical intermediate in organic synthesis. It acts as a substrate or reagent in various reactions, contributing to the formation of new carbon-carbon or carbon-heteroatom bonds. At the molecular level, it participates in nucleophilic substitution, oxidation, or reduction processes, enabling the construction of complex molecular structures. Its mode of action involves serving as a building block for the synthesis of agrochemicals, or materials with specific properties. In the development, it plays a role in the exploration of new chemical entities and the investigation of structure-activity relationships. Its presence in experimental applications allows for the exploration of diverse chemical transformations and the development of novel methodologies.


α-Cyclopropylbenzyl alcohol (CAS 1007-03-0) References

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  2. Oxidant-free alcohol dehydrogenation using a reusable hydrotalcite-supported silver nanoparticle catalyst.  |  Mitsudome, T., et al. 2008. Angew Chem Int Ed Engl. 47: 138-41. PMID: 18038437
  3. Sulfated and sulfonated polysaccharide as chiral stationary phases for capillary electrochromatography and capillary electrochromatography-mass spectrometry.  |  Zheng, J., et al. 2009. J Chromatogr A. 1216: 857-72. PMID: 19108837
  4. Gold(III)-Catalyzed Decarboxylative C3-Benzylation of Indole-3-carboxylic Acids with Benzylic Alcohols in Water.  |  Hikawa, H., et al. 2019. J Org Chem. 84: 1972-1979. PMID: 30672696
  5. HFIP-catalyzed direct dehydroxydifluoroalkylation of benzylic and allylic alcohols with difluoroenoxysilanes.  |  Li, J., et al. 2021. Chem Commun (Camb). 57: 1050-1053. PMID: 33409524
  6. Direct coupling reaction between alcohols and allyltrimethylsilane catalyzed by phosphomolybdic acid  |   and Santosh T. Kadam, Hanbin Lee, Sung Soo Kim. February 2010. Applied Organometallic Chemistry. Volume24, Issue2: Pages 67-70.
  7. Expanding substrate scope of lipase-catalyzed transesterification by the utilization of liquid carbon dioxide  |  HN Hoang, T Matsuda - Tetrahedron, 2016 - Elsevier. November 2016,. Tetrahedron. Volume 72, Issue 46, 17: 7229-7234.
  8. Solvent-free aerobic alcohol oxidation using Cu/Nb2O5: Green and highly selective photocatalytic system  |  S Furukawa, A Tamura, T Shishido, K Teramura… - Applied Catalysis B …, 2011 - Elsevier. 2 November 2011,. Applied Catalysis B: Environmental. Volume 110,: Pages 216-220.
  9. A Radical Pathway for Direct Substitution of Benzyl Alcohols with Water-Soluble Copper Catalyst in Water  |  , et al. March 3, 2016. Advanced Synthesis & Catalysis. Volume358, Issue5: Pages 765-773.
  10. Redox-Active Catalyst Based on Poly(Anilinesulfonic Acid)- Supported Gold Nanoparticles for Aerobic Alcohol Oxidation in Water  |   and Daisuke Saio, Toru Amaya, Toshikazu Hirao. September 10, 2010. Advanced Synthesis & Catalysis. Volume352, Issue13: Pages 2177-2182.
  11. Ligand-free Iron(II)-Catalyzed N-Alkylation of Hindered Secondary Arylamines with Non-activated Secondary and Primary Alcohols via a Carbocationic Pathway  |   and Onkar S. Nayal, Maheshwar S. Thakur, Manoranjan Kumar, Neeraj Kumar, Sushil K. Maurya. February 15, 2018. Advanced Synthesis & Catalysis. Volume360, Issue4: Pages 730-737.
  12. Cobalt(II)/TPPMS-Catalyzed Dehydrative Nucleophilic Substitution of Alcohols in Water  |   and Hidemasa Hikawa, Yukiko Ijichi, Shoko Kikkawa, Isao Azumaya. January 18, 2017. European Journal of Organic Chemistry. Volume2017, Issue3: Pages 465-468.
  13. Dioxygen Activation by a Hexagonal SrMnO3 Perovskite Catalyst for Aerobic Liquid-Phase Oxidation  |   and Shuma Kawasaki, Dr. Keigo Kamata, Prof. Dr. Michikazu Hara. October 20, 2016. ChemCatChem. Volume8, Issue20: Pages 3247-3253.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

α-Cyclopropylbenzyl alcohol, 1 g

sc-227163
1 g
$35.00