1266099-74-4 Usage
Uses
Used in Pharmaceutical Research:
(S)-Benzyl 3-(2-(allyloxy)-2-oxoethoxy)-2-(methylamino)propanoate hydrochloride is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structure and functional groups. Its potential biological activities make it a valuable asset in the development of new drugs with specific therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-benzyl 3-(2-(allyloxy)-2-oxoethoxy)-2-(methylamino)propanoate hydrochloride serves as a versatile building block for the creation of a wide range of chemical products. Its diverse functional groups allow for numerous reactions and modifications, contributing to the synthesis of complex organic molecules with various applications.
Used in Drug Development:
(S)-Benzyl 3-(2-(allyloxy)-2-oxoethoxy)-2-(methylamino)propanoate hydrochloride is used as a starting material for the development of new drugs. Its unique structure and functional groups may exhibit specific biological activities, making it a promising candidate for the creation of pharmaceuticals with targeted therapeutic effects.
Used in the Pharmaceutical Industry:
(S)-Benzyl 3-(2-(allyloxy)-2-oxoethoxy)-2-(methylamino)propanoate hydrochloride is used as a compound with potential applications in the pharmaceutical industry. Its hydrochloride form enhances its solubility in aqueous solutions, making it more suitable for various pharmaceutical applications, such as drug formulation and delivery systems.
Check Digit Verification of cas no
The CAS Registry Mumber 1266099-74-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,6,0,9 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1266099-74:
(9*1)+(8*2)+(7*6)+(6*6)+(5*0)+(4*9)+(3*9)+(2*7)+(1*4)=184
184 % 10 = 4
So 1266099-74-4 is a valid CAS Registry Number.
1266099-74-4Relevant academic research and scientific papers
CONFORMATIONALLY CONSTRAINED, FULLY SYNTHETIC MACROCYCLIC COMPOUNDS
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Page/Page column 116, (2012/11/07)
Conformationally restricted, spatially defined 12-30 membered macrocyclic ring systems of formulae Ia and Ib are constituted by three distinct molecular parts: Template A, conformation Modulator B and Bridge C. These macrocycles Ia and Ib are readily manufactured by parallel synthesis or combinatorial chemistry in solution or on solid phase. They are designed to interact with a variety of specific biological target classes, examples being the agonistic or antagonistic activity on G-protein coupled receptors (GPCRs), ion channels and signal transduction pathways. In particular, these macrocycles act as antagonists of the motilin receptor, the FP receptor and the purinergic receptors P2Y1, as modulators of the serotonin receptor of subtype 5-HT2B, as blockers of the voltage-gated potassium channel Kv1.3 and as inhibitors of the β-catenin-dependent “canonical” Wnt pathway. Thus they are showing great potential as medicaments for a variety of diseases.
