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67031-41-8

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67031-41-8 Usage

General 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 with the chemical formula C12H18O3. It is a secondary alcohol with a phenyl group and two methoxy groups attached to the carbon chain. This chemical can be used as a fragrance ingredient in perfumes and personal care products. It has a floral and woody aroma, making it a popular choice for use in cosmetic and fragrance formulations. Additionally, the compound may also be utilized in the synthesis of other organic compounds due to its unique chemical structure and reactivity.

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.

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