54344-93-3 Usage
Uses
Used in Organic Synthesis:
4-Methoxy-2,3,6-trimethylbenzyl alcohol is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for a wide range of reactions, making it a versatile building block in the development of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Methoxy-2,3,6-trimethylbenzyl alcohol is used as a starting material for the synthesis of various drugs and drug candidates. Its chemical properties enable the creation of novel compounds with potential therapeutic effects, contributing to the development of new medications for various diseases and conditions.
Used in Chemical Research:
4-Methoxy-2,3,6-trimethylbenzyl alcohol is also used in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic pathways. Its unique structure provides researchers with valuable insights into the behavior of similar compounds, furthering the understanding of organic chemistry and its applications.
Used in Flavor and Fragrance Industry:
Due to its distinct chemical properties, 4-Methoxy-2,3,6-trimethylbenzyl alcohol can be used as a component in the creation of various flavors and fragrances. Its unique scent profile can be utilized to develop new and innovative fragrances for the perfume and cosmetic industries, as well as to enhance the taste and aroma of various food products.
Used in Material Science:
In the field of material science, 4-Methoxy-2,3,6-trimethylbenzyl alcohol can be used to develop new materials with specific properties. Its chemical structure can be manipulated to create compounds with unique physical and chemical characteristics, potentially leading to the development of new materials with applications in various industries, such as electronics, automotive, and aerospace.
Check Digit Verification of cas no
The CAS Registry Mumber 54344-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,4 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54344-93:
(7*5)+(6*4)+(5*3)+(4*4)+(3*4)+(2*9)+(1*3)=123
123 % 10 = 3
So 54344-93-3 is a valid CAS Registry Number.
54344-93-3Relevant academic research and scientific papers
Tailoring 3,3'-dihydroxyisorenieratene to hydroxystilbene: Finding a resveratrol analogue with increased antiproliferation activity and cell selectivity
Kang, Yan-Fei,Yan, Wen-Jing,Zhou, Ting-Wen,Dai, Fang,Li, Xiu-Zhuang,Bao, Xia-Zhen,Du, Yu-Ting,Yuan, Cui-Hong,Wang, Hai-Bo,Ren, Xiao-Rong,Liu, Qiang,Jin, Xiao-Ling,Zhou, Bo,Zhang, Jie
, p. 8904 - 8908 (2014/07/22)
Four novel compounds were designed by "tailoring" 3,3'-dihydroxyisorenieratene (a natural carotenoid) based on an isoprene unit retention truncation strategy. Among them, the smallest molecule 1 (2,3,6,2',3',6'-hexamethyl-4,4'-dihydroxy-trans-stilbene) was concisely synthesized in a one-pot Stille-Heck tandem sequence, and surfaced as a promising lead molecule in terms of its selective antiproliferative activity mediated by blocking the NCI-H460 cell cycle in G1 phase. Additionally, theoretical calculations and cell uptake experiments indicate that the unique polymethylation pattern of compound 1 significantly induces a conformational change shift out of planarity and increases its cell uptake and metabolic stability. The observation should be helpful to rationally design resveratrol-inspired antiproliferative agents. Four novel compounds were designed by "tailoring" 3,3'-dihydroxyisorenieratene (a natural carotenoid) based on an isoprene unit retention truncation strategy. Among them, the smallest molecule 1 was concisely synthesized by a one-pot Stille-Heck tandem sequence, and surfaced as a promising lead molecule in terms of its selective antiproliferative activity (see figure).
