69877-88-9 Usage
Uses
Used in Organic Synthesis:
4-Methoxy-2,3,6-trimethylbenzyl Bromide is used as a synthetic intermediate for the creation of various organic compounds. Its application in this field is due to its ability to undergo a range of chemical reactions, such as substitution, addition, and elimination, which are essential in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Methoxy-2,3,6-trimethylbenzyl Bromide is used as a building block for the development of new drugs. Its unique structure allows it to be a versatile component in the design and synthesis of novel pharmaceutical compounds, potentially leading to the discovery of new therapeutic agents.
Used in Chemical Research:
4-Methoxy-2,3,6-trimethylbenzyl Bromide is also employed in chemical research as a model compound to study various reaction mechanisms and to understand the behavior of similar molecules. This helps researchers to develop a deeper understanding of organic chemistry and to design more efficient synthetic routes for the production of target compounds.
Used in Material Science:
In the field of material science, 4-Methoxy-2,3,6-trimethylbenzyl Bromide can be used as a component in the development of new materials with specific properties. Its incorporation into polymers or other materials can potentially alter their physical and chemical characteristics, leading to the creation of materials with improved performance or novel applications.
Check Digit Verification of cas no
The CAS Registry Mumber 69877-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,7 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69877-88:
(7*6)+(6*9)+(5*8)+(4*7)+(3*7)+(2*8)+(1*8)=209
209 % 10 = 9
So 69877-88-9 is a valid CAS Registry Number.
69877-88-9Relevant 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).
