96854-29-4 Usage
Uses
Used in Organic Synthesis:
(2-carboxy-2-((methoxycarbonyl)amino)ethyl)triphenylphosphonium is used as a reactant for the creation of various organic molecules. Its unique structure allows it to participate in a range of chemical reactions, facilitating the synthesis of complex organic compounds.
Used in Chemical Research:
In the field of chemical research, (2-carboxy-2-((methoxycarbonyl)amino)ethyl)triphenylphosphonium serves as a catalyst or reagent. Its ability to act as a cation in certain organic reactions and its triphenylphosphonium group's enhancing effect on reactivity make it a valuable tool for studying and advancing chemical processes.
Used in the Development of New Molecules and Materials:
(2-carboxy-2-((methoxycarbonyl)amino)ethyl)triphenylphosphonium's properties also make it useful in the development of new molecules and materials. Its role as a cation and the stability provided by the triphenylphosphonium group contribute to the creation of innovative materials with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 96854-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,5 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96854-29:
(7*9)+(6*6)+(5*8)+(4*5)+(3*4)+(2*2)+(1*9)=184
184 % 10 = 4
So 96854-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C23H22NO4P.ClH/c1-28-23(27)24-21(22(25)26)17-29(18-11-5-2-6-12-18,19-13-7-3-8-14-19)20-15-9-4-10-16-20;/h2-16,21H,17H2,1H3,(H-,24,25,26,27);1H/t21-;/m1./s1
96854-29-4Relevant academic research and scientific papers
Synthesis and absolute configuration of wybutine, the fluorescent minor base from phenylalanine transfer ribonucleic acids
Itaya,Mizutani,Iida
, p. 1407 - 1414 (2007/10/02)
The phosphonium chloride 6 having an optically active amino acid moiety was synthesized from (S)-serine benzyl ester tosylate (2b) through a six-step route. The utility of 6 as a reagent for the Wittig reaction was exemplified in the olefination with benz
SYNTHESIS OF (S)-(-)-WYBUTINE, THE FLUORESCENT MINOR BASE FROM YEAST PHENYLALANINE TRANSFER RIBONUCLEIC ACIDS
Itaya, Taisuke,Mizutani, Akemi
, p. 347 - 350 (2007/10/02)
The Wittig reaction of 1-benzyl-7-formylwye (12) with (R)-ethyl>triphenylphosphonium chlorid (8) followed by successive methylation and reduction gave (-)-wybutine .
