172900-92-4 Usage
Uses
Used in Pharmaceutical Research:
Carbamic acid, N-[(1S,2S,4S)-2-hydroxy-1-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-5-methyl-4-[(phenylmethoxy)methyl]hexyl]-, 1,1-dimethylethyl ester is used as a research compound for the development of new pharmaceutical agents. Its complex structure and functional groups may offer unique properties that can be harnessed for the creation of novel drugs with specific therapeutic effects.
Used in Chemical Research:
In the field of chemical research, Carbamic acid, N-[(1S,2S,4S)-2-hydroxy-1-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-5-methyl-4-[(phenylmethoxy)methyl]hexyl]-, 1,1-dimethylethyl ester serves as a starting material or intermediate in the synthesis of other complex organic molecules. Its reactivity and structural features make it a valuable component in the development of new chemical entities with potential applications in various industries.
Used in Drug Synthesis:
Carbamic acid, N-[(1S,2S,4S)-2-hydroxy-1-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-5-methyl-4-[(phenylmethoxy)methyl]hexyl]-, 1,1-dimethylethyl ester is used as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows for the formation of new chemical bonds and the creation of molecules with specific biological activities, making it a valuable asset in the development of innovative drugs.
Used in Material Science:
In material science, Carbamic acid, N-[(1S,2S,4S)-2-hydroxy-1-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-5-methyl-4-[(phenylmethoxy)methyl]hexyl]-, 1,1-dimethylethyl ester may be utilized in the development of new materials with unique properties. Its ability to form various chemical bonds and its structural complexity can contribute to the creation of advanced materials with applications in different fields, such as electronics, coatings, or adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 172900-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,9,0 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 172900-92:
(8*1)+(7*7)+(6*2)+(5*9)+(4*0)+(3*0)+(2*9)+(1*2)=134
134 % 10 = 4
So 172900-92-4 is a valid CAS Registry Number.
172900-92-4Relevant academic research and scientific papers
Structural modification of the P2′ position of 2,7-dialkyl- substituted 5(S)-amino-4(S)-hydroxy-8-phenyl-octanecarboxamides: The discovery of aliskiren, a potent nonpeptide human renin inhibitor active after once daily dosing in marmosets
Maibaum, Jürgen,Stutz, Stefan,G?schke, Richard,Rigollier, Pascal,Yamaguchi, Yasuchika,Cumin, Frédéric,Rahuel, Joseph,Baum, Hans-Peter,Cohen, Nissim-Claude,Schnell, Christian R.,Fuhrer, Walter,Gruetter, Markus G.,Schilling, Walter,Wood, Jeanette M.
, p. 4832 - 4844 (2008/03/12)
Due to its function in the rate limiting initial step of the renin-angiotensin system, renin is a particularly promising target for drugs designed to control hypertension, a growing risk to health worldwide. Despite vast efforts over more than two decades
Practical synthesis of an orally active renin inhibitor aliskiren
Dong, Hua,Zhang, Zhi-Liu,Huang, Jia-Hui,Ma, Rujian,Chen, Shu-Hui,Li, Ge
, p. 6337 - 6340 (2007/10/03)
A convergent synthesis of aliskiren was accomplished via the use of Segment AB as the key intermediate, which was prepared via the coupling of the Grignard reagent derived from Segment B with Segment A, followed by subsequent oxidative lactonization.
METHODS OF TREATING ALZHEIMER'S DISEASE USING ARYL ALKANOIC ACID AMIDES
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Page 233, (2010/02/05)
Disclosed are methods for treating Alzheimer’s disease, and other diseases, and/or inhibiting beta-secretase enzyme, and/or inhibiting deposition of A beta peptide in a mammal, by use of compounds of formula 1 (1) wherein the variables R1-R8 and X are defined herein.
