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(3,4-dimethoxy-2-methylphenoxy)methyl methyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1376220-15-3

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1376220-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1376220-15-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,6,2,2 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1376220-15:
(9*1)+(8*3)+(7*7)+(6*6)+(5*2)+(4*2)+(3*0)+(2*1)+(1*5)=143
143 % 10 = 3
So 1376220-15-3 is a valid CAS Registry Number.

1376220-15-3Relevant academic research and scientific papers

Construction of BCDEF Core of Andilesin C

Zhu, Guili,Zhou, Chengying,Chen, Song,Fu, Shaomin,Liu, Bo

supporting information, p. 7809 - 7812 (2019/10/10)

A synthetic study toward the BCDEF core skeleton of andilesin C is presented. Key elements involved iron-promoted intramolecular perezone-type [5 + 2] cycloaddition to install the BCD ring system simultaneously in a one-step, copper-catalyzed intramolecul

Chemistry of renieramycins. Part 12: An improved total synthesis of (±)-renieramycin G

Yokoya, Masashi,Shinada-Fujino, Kimiko,Yoshida, Saiko,Mimura, Masahiro,Takada, Hiroki,Saito, Naoki

experimental part, p. 4166 - 4181 (2012/07/28)

An improved total synthesis of (±)-renieramycin G (1g) from readily available 2-hydroxy-3-methyl-4,5-dimethoxybenzaldehyde (7) in 21 steps (6.3% overall yield) is described. The synthesis features the concise construction of a pentacyclic framework using the stereoselective Pictet-Spengler type cyclization reaction of lactam (25) with ethyl diethoxyacetate, followed by the base-catalyzed epimerization of the C-1 stereo center of aldehyde (30a). The results of cytotoxicity studies are also presented.

Sporolide B: Synthetic studies

Gladding, Jeffery A.,Bacci, James P.,Shaw, Scott A.,Smith III, Amos B.

scheme or table, p. 6697 - 6706 (2011/10/01)

Studies directed toward the synthesis of the architecturally complex marine natural product sporolide B are described. Synthetic analysis suggested advanced hydroquinone and benzodiquinane fragments, which upon elaboration were successfully united via an

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