556038-72-3 Usage
Uses
Used in Organic Synthesis:
(8S)-4-benzyloxy-8-(tert-butyldimethylsilanyloxymethyl)-3,6,7,8-tetrahydro-3,6-diaza-as-indacene-2,3,6-tricarboxylic acid 3-benzyl ester 2-methyl ester 6-(2,2,2-trichloroethyl) ester is used as a synthetic intermediate for the development of novel organic compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of complex molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (8S)-4-benzyloxy-8-(tert-butyldimethylsilanyloxymethyl)-3,6,7,8-tetrahydro-3,6-diaza-as-indacene-2,3,6-tricarboxylic acid 3-benzyl ester 2-methyl ester 6-(2,2,2-trichloroethyl) ester is used as a starting material for the design and synthesis of new drugs. Its multiple functional groups can be exploited to create a variety of bioactive molecules with potential therapeutic applications.
Used in Chemical Research:
(8S)-4-benzyloxy-8-(tert-butyldimethylsilanyloxymethyl)-3,6,7,8-tetrahydro-3,6-diaza-as-indacene-2,3,6-tricarboxylic acid 3-benzyl ester 2-methyl ester 6-(2,2,2-trichloroethyl) ester is utilized in chemical research to study the reactivity and properties of its various functional groups. This can lead to a better understanding of its potential applications and the development of new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 556038-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,0,3 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 556038-72:
(8*5)+(7*5)+(6*6)+(5*0)+(4*3)+(3*8)+(2*7)+(1*2)=163
163 % 10 = 3
So 556038-72-3 is a valid CAS Registry Number.
556038-72-3Relevant academic research and scientific papers
Total synthesis of the duocarmycins
Yamada, Ken,Kurokawa, Toshiki,Tokuyama, Hidetoshi,Fukuyama, Tohru
, p. 6630 - 6631 (2007/10/03)
The total synthesis of (+)-duocarmycin A and SA through a common indoline intermediate is described. The key reactions include selective lithiation of a 2,6-dibromoiodobenzene derivative and diastereoselective addition to a chiral nitroalkene, copper-mediated aryl amination, and addition of aryllithium to azlactones. Copyright
