1093192-06-3 Usage
Description
(S)-methyl 3-(tert-butoxycarbonylamino)-3-methyl-2-((S)-1-phenylethylamino)butanoate is a complex chemical compound derived from the amino acid leucine. It features additional groups attached to its amino and carboxyl functional groups, making it a versatile chiral building block in organic synthesis and pharmaceutical research. Its unique structural features and stereochemical properties contribute to its potential in the development of new drugs and therapeutic agents, as well as applications in peptide chemistry and as a reagent in asymmetric synthesis.
Uses
Used in Pharmaceutical Research:
(S)-methyl 3-(tert-butoxycarbonylamino)-3-methyl-2-((S)-1-phenylethylamino)butanoate is used as a chiral building block for the synthesis of biologically active compounds. Its unique stereochemistry allows for the creation of enantiomerically pure compounds, which is crucial for the development of new drugs and therapeutic agents with improved efficacy and reduced side effects.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-methyl 3-(tert-butoxycarbonylamino)-3-methyl-2-((S)-1-phenylethylamino)butanoate serves as a valuable intermediate for the preparation of various complex organic molecules. Its reactivity and functional group compatibility make it suitable for a wide range of synthetic transformations, facilitating the construction of diverse molecular architectures.
Used in Peptide Chemistry:
(S)-methyl 3-(tert-butoxycarbonylamino)-3-methyl-2-((S)-1-phenylethylamino)butanoate is utilized in peptide chemistry as a non-natural amino acid for the synthesis of peptide-based drugs and bioactive peptides. Its incorporation into peptide sequences can modulate the properties of the resulting peptides, such as stability, bioavailability, and target specificity.
Used in Asymmetric Synthesis:
As a reagent in asymmetric synthesis, (S)-methyl 3-(tert-butoxycarbonylamino)-3-methyl-2-((S)-1-phenylethylamino)butanoate plays a crucial role in the enantioselective formation of chiral centers in target molecules. Its use in this context can enhance the efficiency and selectivity of synthetic processes, leading to the production of enantiomerically pure compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1093192-06-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,1,9 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1093192-06:
(9*1)+(8*0)+(7*9)+(6*3)+(5*1)+(4*9)+(3*2)+(2*0)+(1*6)=143
143 % 10 = 3
So 1093192-06-3 is a valid CAS Registry Number.
1093192-06-3Relevant articles and documents
COMPOUND ACTING AS ANTIBIOTICS
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, (2020/12/22)
The present invention provides a novel antibiotic compound represented by the following formula (I), a pharmaceutically acceptable salt thereof, an ester thereof, a prodrug thereof, a solvate thereof, or a deuterated analog thereof, or a stereoisomer thereof. The compound of the present invention exhibits excellent antibacterial activity, especially against Gram bacteria. wherein each group is defined as in the description.
ETHYNYLBENZENE DERIVATIVES
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, (2012/03/26)
Disclosed are compounds of formulae (I), (II), and (II)I: and pharmaceutically acceptable salts thereof, wherein the variables, R, R1, R2, R3, R101, L, D, Q, Y, X, and Z are defined herein. These compounds are useful for treating Gram-negative bacteria infections.
