129034-70-4 Usage
Uses
Used in Pharmaceutical Industry:
3-Isopropoxy-4-(tributylstannyl)-1,2-cyclobutenedione Liebeskind Reagent is used as a pharmaceutical intermediate for the synthesis of various drugs and drug candidates. Its unique structure allows for the formation of new chemical bonds and the creation of diverse molecular architectures, which can be tailored to target specific biological pathways or receptors.
The application of this reagent in the pharmaceutical industry is primarily due to its ability to facilitate cross-coupling reactions, which are essential for the formation of carbon-carbon and carbon-heteroatom bonds in complex organic molecules. These reactions are crucial for the synthesis of many biologically active compounds, including those with potential therapeutic applications.
In addition to its role as a pharmaceutical intermediate, 3-Isopropoxy-4-(tributylstannyl)-1,2-cyclobutenedione Liebeskind Reagent may also find applications in other industries, such as:
Used in Chemical Research:
In the field of chemical research, this reagent can be employed as a tool for exploring new reaction pathways and developing innovative synthetic methods. Its unique properties make it a valuable asset for chemists working on the design and synthesis of novel organic compounds with potential applications in various fields, including materials science, agrochemistry, and environmental science.
Used in Material Science:
3-Isopropoxy-4-(tributylstannyl)-1,2-cyclobutenedione Liebeskind Reagent may also be utilized in the development of new materials with specific properties, such as improved stability, enhanced reactivity, or unique optical, electronic, or mechanical characteristics. These materials could have potential applications in a wide range of industries, from electronics and energy to aerospace and automotive.
Check Digit Verification of cas no
The CAS Registry Mumber 129034-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,3 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129034-70:
(8*1)+(7*2)+(6*9)+(5*0)+(4*3)+(3*4)+(2*7)+(1*0)=114
114 % 10 = 4
So 129034-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7O3.3C4H9.Sn/c1-4(2)10-6-3-5(8)7(6)9;3*1-3-4-2;/h4H,1-2H3;3*1,3-4H2,2H3;/rC19H34O3Sn/c1-6-9-12-23(13-10-7-2,14-11-8-3)19-17(21)16(20)18(19)22-15(4)5/h15H,6-14H2,1-5H3
129034-70-4Relevant academic research and scientific papers
SUBSTITUTED TETRACYCLINE COMPOUNDS FOR TREATMENT OF INFLAMMATORY SKIN DISORDERS
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Page/Page column 34, (2008/12/07)
Methods and compositions for the treatment of skin disorders (e.g., acne, rosacea) are described.
Antibiotic C-3 cyclobutenedione substituted (1-carba)cephalosporin compounds, compositions, and methods of use thereof
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, (2008/06/13)
A compound of formula I STR1 wherein X is sulfur or CH2 ; R1 is hydrogen, hydroxy, amino, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, phenyl optionally substituted with one to three C1-6 alkyl, C1-6 alkyloxy or hydroxy, C1-6 alkylthio, phenylthio optionally substituted with one to three C1-6 alkyl or C1-6 alkyloxy on the phenyl ring, phenylmethyloxy optionally substituted with one to three C1-6 alkyl or C1-6 alkyloxy on the phenyl ring, 1-morpholino, C1-6 alkyloxy, C2-6 alkenylmethyloxy, C3-6 alkynylmethyloxy, C1-6 alkylamino, C1-6 dialkylamino or a radical selected from the group consisting of STR2 in which n is 0 to 3, R5 is C1-6 alkyl or hydrogen, and R3 and R4 are independently C1-6 alkyl; R2 is hydrogen, a conventional amino protecting group or an acyl group; R0 is hydrogen or a conventional carboxy protecting group, or --CO2 R0 taken together forms a physiologically hydrolyzable ester; or pharmaceutically acceptable salts or solvates thereof.
