1023648-23-8 Usage
Chemical structure
2-(2-[4-(3-benzyloxy-phenylsulfanyl)-2-chloro-phenyl]-ethyl)-2-methoxy-malonic acid dimethyl ester is a complex organic compound with a combination of functional groups.
Functional groups
The compound contains sulfanyl, chloro, methoxy, and ester groups, which contribute to its chemical reactivity and potential applications.
Ester structure
It is a dimethyl ester of 2-(2-[4-(3-benzyloxy-phenylsulfanyl)-2-chloro-phenyl]-ethyl)-2-methoxy-malonic acid, indicating the presence of two ester groups.
Organic synthesis and pharmaceutical research
The compound is commonly used in these fields, suggesting its versatility and potential for further development.
Potential applications in medicinal chemistry
The structural features and functional groups of the compound make it a promising candidate for the development of new drug candidates or as a reference compound for analytical purposes.
Benzyloxy and chloro groups
The presence of these groups in the molecule makes it an interesting target for further study, potentially leading to the development of new chemical reactions or synthesis methods.
Check Digit Verification of cas no
The CAS Registry Mumber 1023648-23-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,3,6,4 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1023648-23:
(9*1)+(8*0)+(7*2)+(6*3)+(5*6)+(4*4)+(3*8)+(2*2)+(1*3)=118
118 % 10 = 8
So 1023648-23-8 is a valid CAS Registry Number.
1023648-23-8Relevant articles and documents
An efficient total synthesis of a sphingosine-1-phosphate receptor agonist KRP-203
Chino, Masao,Kiuchi, Masatoshi,Adachi, Kunitomo
, p. 3859 - 3866 (2008/09/21)
An efficient total synthesis of the S1P1 agonist, KRP-203, is described. The key step involves the conjugate addition of diethyl acetamidomalonate to a styrene compound to give the core structure of KRP-203. Multigram quantities of the targeted KRP-203, sufficient for several biological studies, were obtained in six steps with an overall yield of 58%.
