30698-18-1 Usage
Uses
Used in Organic Synthesis:
(3-(Benzoyloxy)propyl)triphenylphosphonium bromide is used as a phase-transfer catalyst for facilitating the transfer of ions between different phases in organic synthesis processes. Its ability to bridge reactions across phase boundaries enhances the efficiency and selectivity of various chemical transformations.
Used in Cancer Treatment Research:
In the field of oncology, (3-(Benzoyloxy)propyl)triphenylphosphonium bromide is studied for its potential as an anticancer agent. It is used for its capacity to selectively accumulate in tumor cells, where it can induce cell death, offering a targeted approach to cancer treatment.
Used in Pharmaceutical Compound Preparation:
(3-(BENZOYLOXY)PROPYL)TRIPHENYLPHOSPHONIUM BROMIDE is utilized in the preparation of various pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Biochemical Research:
(3-(Benzoyloxy)propyl)triphenylphosphonium bromide is also employed in biochemical research, where it aids in studying cellular processes and interactions, particularly those related to its effects on tumor cells.
Check Digit Verification of cas no
The CAS Registry Mumber 30698-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,9 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30698-18:
(7*3)+(6*0)+(5*6)+(4*9)+(3*8)+(2*1)+(1*8)=121
121 % 10 = 1
So 30698-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C28H26O2P/c29-28(24-14-5-1-6-15-24)30-22-13-23-31(25-16-7-2-8-17-25,26-18-9-3-10-19-26)27-20-11-4-12-21-27/h1-12,14-21H,13,22-23H2/q+1
30698-18-1Relevant academic research and scientific papers
Stereoselective synthesis of 3-oxygenated-ds-dialkyl-2,5-substituted tetrahydrofurans from cyclohexadienediols
Brovetto, Margarita,Seoane, Gustavo
, p. 5776 - 5785 (2008/12/21)
(Chemical Equation Presented) The 3-oxygenated-cis-dialkyl-2,5-substituted tetrahydrofuran system, present in several natural products, was prepared with good selectivity by acidic cyclization of 5-alkene-1,2,4-triol derivatives. The starting alkenol was
