116261-30-4 Usage
Uses
Used in Pharmaceutical Industry:
trans-(±)-Dihydro-3,4-bis[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone is used as a precursor for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of chemical synthesis, trans-(±)-Dihydro-3,4-bis[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone serves as an intermediate or building block for the creation of more complex molecules. Its versatility in chemical reactions makes it a valuable component in the synthesis of various compounds.
Used in Material Science:
trans-(±)-Dihydro-3,4-bis[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone can be utilized in the development of new materials with specific properties. Its chemical structure may contribute to the enhancement of material characteristics such as strength, durability, or thermal stability.
Used in Cosmetics Industry:
Due to its potential antioxidant and anti-inflammatory properties, trans-(±)-Dihydro-3,4-bis[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone may be used as an active ingredient in the cosmetics industry. It could be incorporated into skincare products for its potential benefits to the skin.
Used in Research and Development:
As a novel compound, trans-(±)-Dihydro-3,4-bis[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone holds potential for further research and development. It can be studied for its properties, interactions with other compounds, and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 116261-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,6 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116261-30:
(8*1)+(7*1)+(6*6)+(5*2)+(4*6)+(3*1)+(2*3)+(1*0)=94
94 % 10 = 4
So 116261-30-4 is a valid CAS Registry Number.
116261-30-4Relevant academic research and scientific papers
A novel approach towards dibenzylbutyrolactone lignans involving heck and radical reactions: Application to (±)-matairesinol synthesis
Singh, Rekha,Singh, Gobind C.,Ghosh, Sunil K.
, p. 5376 - 5385 (2008/03/14)
A highly regio- and stereoselective Heck reaction of iodoarenes with vinylated malonates, generated in situ by fluoride-induced protiodesilylation of alkenylsilanols/disiloxanes to give functionalized styrenes and 1,4-diaryl-1-butenes has been developed. The dibenzylbutyrolactone lignan skeletons have been achieved from 1,4-diaryl-1-butenes by two routes involving diastereoselective radical cyclization as the key step. This strategy has successfully been applied in the synthesis of (±)-matairesinol. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
Total Synthesis of (+/-)-Wikstromol
Belletire,John L.,Fry,Douglas F.
, p. 4724 - 4729 (2007/10/02)
The antineoplastic prototype lignan natural product wikstromol was synthesized in racemic form by a straightforward sequence involving, as its key transformations,oxidative coupling of a carboxylic acid dianion,generation and stereoselective oxidation of a potassium enolate,and a deprotection step.The overall yield for nine steps is 29percent.Depending on the choice of oxidants for the enolate,considerable modification in the ratio of stereoisomeric products is possible.
