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(+/-)-1-(2,5-Dimethoxyphenyl)butan-3-ol is a chiral chemical compound with the molecular formula C12H18O3. It features a butyl chain attached to a chiral center and two methoxy groups on the phenyl ring, giving it unique properties. This secondary alcohol is known for its optical activity, with one enantiomer being active and the other inactive. Its stereochemistry and functional groups make it a valuable building block in organic synthesis and chemical research.

147249-35-2

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147249-35-2 Usage

Uses

Used in Organic Synthesis:
(+/-)-1-(2,5-Dimethoxyphenyl)butan-3-ol is used as a key intermediate in organic synthesis for the creation of more complex molecules. Its unique structure and functional groups allow for versatile reactions and the development of new compounds with potential applications across various industries.
Used in Chemical Research:
In the field of chemical research, (+/-)-1-(2,5-Dimethoxyphenyl)butan-3-ol serves as a valuable compound for studying stereochemistry, reaction mechanisms, and the properties of secondary alcohols. Its optical activity and chiral nature make it an interesting subject for investigations into enantioselective synthesis and the effects of stereochemistry on chemical behavior.
Used in Pharmaceutical Industry:
(+/-)-1-(2,5-Dimethoxyphenyl)butan-3-ol is used as a building block in the pharmaceutical industry for the synthesis of potential drug candidates. Its unique structure and functional groups may contribute to the development of new medications with novel mechanisms of action or improved pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical industry, (+/-)-1-(2,5-Dimethoxyphenyl)butan-3-ol may be utilized for the development of new pesticides, herbicides, or other agricultural chemicals. Its potential biological activity and structural features could lead to the creation of more effective and targeted agrochemicals.
Potential for Further Studies:
Due to its unique properties and potential biological activity, (+/-)-1-(2,5-Dimethoxyphenyl)butan-3-ol may be of interest for further studies in various fields, including medicinal chemistry, materials science, and environmental chemistry. Its exploration could lead to new discoveries and applications that have yet to be realized.

Check Digit Verification of cas no

The CAS Registry Mumber 147249-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,4 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 147249-35:
(8*1)+(7*4)+(6*7)+(5*2)+(4*4)+(3*9)+(2*3)+(1*5)=142
142 % 10 = 2
So 147249-35-2 is a valid CAS Registry Number.

147249-35-2Relevant academic research and scientific papers

High pressure nucleophilic fluoride-ion substitution reactions: Formation of fluoroalkylbenzenes

Gerdes, John M.,Keil, Robert N.,Shulgin, Alexander T.,Mathis, Chester A.

, p. 121 - 129 (2007/10/03)

A series of 1-phenyl-2-tosyloxy- and 1-phenyl-3-tosyloxyalkanes was synthesized and then subjected to tetrabutylammonium fluoride in THF under 15 kbar (1.5 GPa), 8 kbar or 1 bar pressures. The resultant substitution and elimination reaction product distributions were analyzed. The application of pressure enhanced the progress of the fluoride-ion substitution reactions. The degree of selectivity of the one reaction over the other was found to be a function of tosylate substrate structure and the amount of pressure applied. The exclusive formation of fluoroalkanes from 1-phenyl-2-tosyloxyalkane substrates under 15 kbar pressure demonstrated the potential of the pressure method for prospective use in fluorine-18 radiolabelling applications.

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