10602-02-5 Usage
Uses
Used in Organic Synthesis:
(p-Carboxyphenyl)-propiolsaeure is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the formation of a wide range of derivatives, making it a valuable asset in the development of novel chemical entities.
Used in Chemical Research:
In the realm of chemical research, (p-Carboxyphenyl)-propiolsaeure is employed as a vital component in the exploration of new reaction pathways and mechanisms. Its reactivity and structural properties contribute to a deeper understanding of chemical processes and the potential for new discoveries.
Used in Pharmaceutical Development:
(p-Carboxyphenyl)-propiolsaeure has garnered interest for its potential use in the development of pharmaceuticals. Its unique structure and reactivity make it a promising candidate for the design of new drugs, particularly in the areas of medicinal chemistry and drug design.
Used as a Reagent in Organic Chemical Reactions:
(p-Carboxyphenyl)-propiolsaeure is also used as a reagent in various organic chemical reactions. Its ability to participate in a range of reactions, such as esterification, amidation, and condensation, makes it a versatile tool in the synthesis of complex organic molecules.
Used in Materials Science:
(p-Carboxyphenyl)-propiolsaeure has been investigated for its potential applications in materials science. Its unique properties and reactivity offer opportunities for the development of new functional materials with tailored properties for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10602-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,6,0 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10602-02:
(7*1)+(6*0)+(5*6)+(4*0)+(3*2)+(2*0)+(1*2)=45
45 % 10 = 5
So 10602-02-5 is a valid CAS Registry Number.
10602-02-5Relevant academic research and scientific papers
Copper catalysed domino decarboxylative cross coupling-cyclisation reactions: Synthesis of 2-arylindoles
Ponpandian, Thanasekaran,Muthusubramanian, Shanmugam
supporting information; experimental part, p. 4248 - 4252 (2012/08/28)
The efficient synthesis of 2-arylindoles and 6H-isoindolo[2,1-a]indol-6-one through copper catalysed domino sp-sp2 decarboxylative cross-coupling and subsequent cyclisation reactions of arylpropiolic acids with 2-iodotrifluoroacetanilide has been described. This methodology also demonstrates that indolo[1,2-c]quinazolin-6(5H)-one can be obtained with the elimination of trifluoromethyl anion.
AN IMPROVED PROCEDURE FOR THE GENERATION AND SELECTIVE TRAPPING OF 2,4'-DILITHIOPHENYLETHYNE
Furber, Mark,Taylor, Richard J. K.,Burford, S. Cliff
, p. C35 - C38 (2007/10/02)
2,4'-Dilithiophenylethyne, prepared by treatment of 4-bromophenylethyne with two equivalents of butyllithium, reacts selectively with electrophilic reagents at the 4'-position provided the correct temperature and solvent combination are employed.The successive addition of two different electrophiles gives the 2,4'-dialkylated product in a regioselective manner.
