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(R)-(E)-2-(3,4,5-trimethoxybenzylidene)-3-[1-(3,4,5-trimethoxyphenyl)-methyl]butanolide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146236-41-1

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146236-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146236-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,2,3 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 146236-41:
(8*1)+(7*4)+(6*6)+(5*2)+(4*3)+(3*6)+(2*4)+(1*1)=121
121 % 10 = 1
So 146236-41-1 is a valid CAS Registry Number.

146236-41-1Downstream Products

146236-41-1Relevant academic research and scientific papers

Process for the preparation of polycyclic compounds using ferric perchlorate and acid trifluoroacidic

-

, (2008/06/13)

Polycyclic compounds (I) can be prepared in accordance with the following reaction formula: STR1 wherein R1 -R8 each represents a hydrogen atom, a hydroxyl group, an alkoxyl group or a substituted or unsubstituted benzyloxy group or

Polycyclic compounds, their preparation and their use as phosphodiesterases inhibitors

-

, (2008/06/13)

Polycyclic compounds (I) can be prepared in accordance with the following reaction formula: wherein R1-R8 each represents a hydrogen atom, a hydroxyl group, an alkoxyl group or a substituted or unsubstituted benzyloxy group or neighb

Synthesis of optically pure gomisin A and schizandrin: The first total synthesis of gomisin A and schizandrin having naturally occurring configurations

Tanaka,Mukaiyama,Mitsuhashi,Wakamatsu

, p. 4165 - 4168 (2007/10/02)

The total synthesis of gomisin A and schizandrin having natural configurations were accomplished for the first time. The key feature of these syntheses is a highly efficient intramolecular oxidative coupling of the intermediates 9 and 21, which can be obtained as both enantiomers in optically pure forms. The manipulation of the lactone moieties of 7 and 22 afforded natural enantiomers of schizandrin and gomisin A.

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