67031-41-8 Usage
Description
1-(3,4-Dimethoxyphenyl)-2-methyl-1-propanol, also known as 3,4-Dimethoxy-α-methyl-β-(1-methylethyl)phenethyl alcohol, is an organic compound characterized by its unique chemical structure featuring a secondary alcohol with a phenyl group and two methoxy groups attached to the carbon chain. It is defined by its chemical formula C12H18O3 and is recognized for its distinct floral and woody aroma.
Uses
Used in Fragrance Industry:
1-(3,4-Dimethoxyphenyl)-2-methyl-1-propanol is used as a fragrance ingredient for its floral and woody aroma, making it a popular choice in the creation of perfumes and personal care products. Its unique scent profile contributes to the overall appeal and character of these products, enhancing the sensory experience for consumers.
Used in Cosmetic Industry:
In the cosmetic industry, 1-(3,4-Dimethoxyphenyl)-2-methyl-1-propanol is utilized as an ingredient for its pleasant scent and ability to blend well with other components in cosmetic formulations. Its inclusion in these products helps to create a more enjoyable and luxurious experience for users.
Used in Organic Synthesis:
Due to its unique chemical structure and reactivity, 1-(3,4-Dimethoxyphenyl)-2-methyl-1-propanol may also be employed in the synthesis of other organic compounds. Its versatility in chemical reactions allows it to serve as a valuable building block or intermediate in the development of various chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 67031-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,3 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67031-41:
(7*6)+(6*7)+(5*0)+(4*3)+(3*1)+(2*4)+(1*1)=108
108 % 10 = 8
So 67031-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O3/c1-8(2)12(13)9-5-6-10(14-3)11(7-9)15-4/h5-8,12-13H,1-4H3
67031-41-8Relevant articles and documents
Copper-catalyzed iminohalogenation of γ, δ-unsaturated oxime esters with halide salts: Synthesis of 2-halomethyl pyrrolines
Chen, Chen,Ding, Jie,Wang, Yuebo,Shi, Xiaonan,Jiao, Dequan,Zhu, Bolin
supporting information, (2019/08/13)
A copper-catalyzed iminohalogenation of unactivated alkenes of γ, δ-unsaturated oxime esters is achieved by using readily available halide salts. Utilizing this protocol, a sequence of structurally diversiform 2-halomethyl pyrrolines are efficiently synthesized and a mechanism involving iminyl radical intermediates, which were initiated by Cu(I) species, was proposed.
FUNGICIDAL COMPOSITION CONTAINING ACID AMIDE DERIVATIVE
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Page/Page column 99-100, (2008/06/13)
Conventional many fungicidal compositions have had practical problems such that either a preventive effect or a curing effect is inadequate, the residual effect tends to be inadequate, or the controlling effect against plant diseases tends to be inadequat
Enzyme-mediated synthesis of (S)- And (R)-verapamil
Brenna, Elisabetta,Fuganti, Claudio,Grasselli, Piero,Serra, Stefano
, p. 1349 - 1357 (2007/10/03)
A lipase-mediated synthesis of (S)- And (R)-verapamil is described. The key steps of the synthetic sequence are the enantioselective acetylation, mediated by Lipase PS, of allylic alcohol (Z)-(±)-2, affording the acetate derivative (Z,R)-(-)-3 (ee 92%) and the Ireland-Claisen rearrangement of this latter and of its enantiomer (Z,S)-(+)-3 (ee 92%) to afford acid derivatives (E,R)-(-)-4 (ee 94%) and (E,S)-(+)-4 (ee 93%), precursors of (S)- and (R)-verapamil, respectively.