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2-(4-Allyl-2,6-dimethoxyphenoxy)-1-(3,4,5-trimethoxyphenyl)-1-propanol is a complex organic compound with a molecular formula of C22H28O7. It is characterized by a propanol backbone, with a 3,4,5-trimethoxyphenyl group attached to the 1-position and a 4-allyl-2,6-dimethoxyphenoxy group attached to the 2-position. This molecule features a combination of hydroxyl, methoxy, and allyl functional groups, which contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. The specific arrangement of these functional groups and the overall molecular structure may influence its reactivity, solubility, and potential interactions with other molecules, making it a compound of interest for further research and development.

41551-58-0

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41551-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41551-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,5 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41551-58:
(7*4)+(6*1)+(5*5)+(4*5)+(3*1)+(2*5)+(1*8)=100
100 % 10 = 0
So 41551-58-0 is a valid CAS Registry Number.

41551-58-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-raphidecursinol

1.2 Other means of identification

Product number -
Other names 2-(4-Allyl-2,6-dimethoxy-phenoxy)-1-(3,4,5-trimethoxy-phenyl)-propan-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:41551-58-0 SDS

41551-58-0Downstream Products

41551-58-0Relevant academic research and scientific papers

A new shortcut synthesis route for (±)raphidecursinol

Yuan, Hua Jie,Cheng, Yao Yao,Qian, Shan,Xiao, Xiang,Wu, Yong

scheme or table, p. 127 - 130 (2010/11/18)

The new shortcut synthesis route of (±)raphidecursinol 1, a racemic 8,4′-oxyneolignan compound, can be more easily achieved by the synthesis route, starting from readily available inexpensive 3,4,5-trimethoxy-benzaldehyde and 1,2,3-trihydroxybenzene. All structures were confirmed by 1H NMR, IR and MS.

In vitro evaluation of antifungal properties of 8.O.4'-Neolignans

Zacchino, Susana,Rodriguez, Gladis,Pezzenati, German,Orellana, Gabriela,Enriz, Ricardo,Sierra, Manuel Gonzalez

, p. 659 - 662 (2007/10/03)

Eighteen racemic 8.O.4'-neolignans with six different substitution patterns in rings A and B, in their ketone and in their erythro and threo alcoholic forms, were evaluated for antifungal activity by the agar dilution method. Only the alcohols exhibited a broad spectrum of activities against Microsporum canis, Microsporum gypseum, Tricophyton mentagrophytes, Tricophyton rubrum, and Epidermophyton floccosum. (±)-erythro-3,4- (methylenedioxy)-7-hydroxy-1'-allyl-3',5'-dimethoxy-8.O.4'-neolignan (11) was the most active compound in the series, and E. floccosum was the most susceptible species.

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