18729-48-1 Usage
Description
3-METHYLCYCLOPENTANOL is a clear, colorless liquid that serves as a versatile intermediate in the synthesis of various chemical compounds. It is a cycloalkanol derivative, which means it contains a cyclopentane ring with a methyl group attached to one of the carbon atoms. This unique structure allows it to be used in the production of a range of products.
Uses
Used in Chemical Synthesis:
3-METHYLCYCLOPENTANOL is used as a key intermediate in the synthesis of various chemical compounds, such as pentacycloalkoxy-substituted phosphazenes and 3-methyl cyclopentylbromide. Its unique structure and reactivity make it a valuable building block for creating complex molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-METHYLCYCLOPENTANOL can be used as a starting material for the development of new drugs. Its ability to form a cyclopentane ring with a methyl group makes it a potential candidate for the synthesis of novel therapeutic agents.
Used in Flavor and Fragrance Industry:
3-METHYLCYCLOPENTANOL, due to its unique chemical structure, can be used as a component in the creation of various flavors and fragrances. Its clear, colorless liquid form makes it suitable for use in the development of new scents and tastes for the consumer market.
Used in Research and Development:
3-METHYLCYCLOPENTANOL can be employed in research and development laboratories to study its chemical properties and potential applications. Its unique structure and reactivity make it an interesting subject for scientific investigation, which could lead to the discovery of new compounds and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 18729-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,2 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18729-48:
(7*1)+(6*8)+(5*7)+(4*2)+(3*9)+(2*4)+(1*8)=141
141 % 10 = 1
So 18729-48-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O/c1-5-2-3-6(7)4-5/h5-7H,2-4H2,1H3/t5-,6-/m0/s1
18729-48-1Relevant articles and documents
Haber,Fuchs
, p. 1447 (1966)
The Stereoselective Reductions of Ketones to the Most Thermodynamically Stable Alcohols Using Lithium and Hydrated Salts of Common Transition Metals
Kennedy, Nicole,Cohen, Theodore
, p. 8134 - 8141 (2015/09/02)
A simple method is presented for the highly stereoselective reductions of ketones to the most thermodynamically stable alcohols. In this procedure, the ketone is treated with lithium dispersion and either FeCl2·4H2O or CuCl2·2H2O in THF at room temperature. This protocol is applied to a large number and variety of ketones and is both more convenient and efficient than those commonly reported for the diastereoselective reduction of five- and six-membered cyclic ketones.
Lanthanide replacement in organic synthesis: Luche-type reduction of α,β-unsaturated ketones in the presence of calcium triflate
Forkel, Nina V.,Henderson, David A.,Fuchter, Matthew J.
supporting information; scheme or table, p. 2129 - 2132 (2012/09/08)
Development of a calcium-mediated regioselective 1,2-reduction of challenging α,β-unsaturated ketones, such as 2-cyclopententone, is reported. The corresponding allylic alcohols are obtained in very good regioselectivities using Ca(OTf)2 and NaBH4. Furthermore, we have shown that our method can stereoselectively reduce aziridinyl ketones.
