1005495-74-8 Usage
Uses
Used in Pharmaceutical Applications:
C43H64N4O4 is used as a pharmaceutical compound for its potential therapeutic properties. The specific application and reason for its use would depend on the compound's properties, such as its ability to interact with biological targets or modulate certain pathways.
Used in Polymer Industry:
C43H64N4O4 is used as a monomer or building block in the synthesis of polymers for various applications. Its unique structure and functional groups may contribute to the development of new materials with specific properties, such as improved strength, flexibility, or chemical resistance.
Used in Other Industrial Applications:
Depending on its specific properties, C43H64N4O4 may have potential uses in other industries, such as in the development of new materials, coatings, or additives. The exact application and reason for its use would be determined by the compound's characteristics and the requirements of the specific industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1005495-74-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,5,4,9 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1005495-74:
(9*1)+(8*0)+(7*0)+(6*5)+(5*4)+(4*9)+(3*5)+(2*7)+(1*4)=128
128 % 10 = 8
So 1005495-74-8 is a valid CAS Registry Number.
1005495-74-8Relevant academic research and scientific papers
Enantioselective Synthesis of 2,2,3-Trisubstituted Indolines via Bimetallic Relay Catalysis of α-Diazoketones with Enones
Yang, Jian,Ke, Chaoqi,Zhang, Dong,Liu, Xiaohua,Feng, Xiaoming
, p. 4536 - 4539 (2018/08/07)
An efficient asymmetric intramolecular trapping of ammonium ylides of α-diazoketones with enones to synthesize indoline derivatives was realized. A Rh(II)/chiral N,N′-dioxide-Sc(III) complex bimetallic relay catalytic system was established. A series of optically active 2,2,3-trisubstituted indolines were obtained in high yields (up to 99%), good enantioselectivities (up to 99% ee), and excellent diastereoselectivities (up to >19:1 dr) under mild reaction conditions.
A catalytic asymmetric ring-expansion reaction of isatins and α-alkyl-α-diazoesters: Highly efficient synthesis of functionalized 2-quinolone derivatives
Li, Wei,Liu, Xiaohua,Hao, Xiaoyu,Cai, Yunfei,Lin, Lili,Feng, Xiaoming
, p. 8644 - 8647 (2012/09/22)
Asymmetric expansion: A catalytic asymmetric ring-expansion reaction of the title compounds occurs in the presence of a Sc(OTf)3 catalyst bearing an N,N?-dioxide-based ligand. Highly functionalized 2-quinolone derivatives containing a chiral C4-quaternary stereocenter were obtained in high yields and high levels of selectivity under mild reaction conditions (see scheme; Tf=trifluoromethanesulfonyl).
