92760-72-0 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-2-AMINO-2-METHYL-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with enhanced efficacy and selectivity.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-2-AMINO-2-METHYL-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE is used as a building block for the creation of complex organic molecules, facilitating the construction of diverse chemical libraries.
Used in Asymmetric Synthesis:
As a chiral auxiliary, (S)-2-AMINO-2-METHYL-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE is used in asymmetric synthesis to induce enantioselectivity, enabling the production of enantiomerically pure compounds, which is crucial in the pharmaceutical and agrochemical industries.
Used in Antifungal and Antitumor Applications:
(S)-2-AMINO-2-METHYL-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE is used as an active ingredient in antifungal and antitumor treatments due to its inherent bioactivity against fungi and tumor cells, respectively.
Used in Peptide Drug Preparation:
In the preparation of peptide drugs, (S)-2-AMINO-2-METHYL-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE is used as a component to construct peptide sequences with specific biological activities, contributing to the development of therapeutic peptides.
Check Digit Verification of cas no
The CAS Registry Mumber 92760-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,6 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92760-72:
(7*9)+(6*2)+(5*7)+(4*6)+(3*0)+(2*7)+(1*2)=150
150 % 10 = 0
So 92760-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2.ClH/c1-4-6(2,7)5(8)9-3;/h4,7H2,1-3H3;1H/t6-;/m0./s1
92760-72-0Relevant articles and documents
Enantiomer mixture and preparation method and application thereof
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Paragraph 0085; 0086; 0087, (2019/06/11)
The invention provides an enantiomer mixture and a preparation method and application thereof, and belongs to the technical field of pesticide chemistry and organic synthesis. The enantiomer mixture is a mixture of S-zoxamide and R-zoxamide, and the enant
N-acetonylbenzamide fungicides
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, (2008/06/13)
This invention relates to new compositions comprising predominantly one enantiomer of an N-acetonylbenzamide fungicide, methods of preparing N-acetonylbenzamides, and their use as fungicides.
The first water-soluble 310-helical peptides
Formaggio, Fernando,Crisma, Marco,Rossi, Paola,Scrimin, Paolo,Kaptein, Bernard,Broxterman, Quirinus B.,Kamphuis, Johan,Toniolo, Claudio
, p. 4498 - 4504 (2007/10/03)
Two water-soluble 310-helical peptides are synthesized and fully characterized for the first time. The sequence of these terminally blocked heptamers comprises two residues of the Cα-trisubstituted α-amino acid 2-amino-3-[1-(1,4,7 triazacyclononyl)]propanoic acid and five residues of a Cα-tetrasubstituted α-amino acid (either α-aminoisobutyric acid or isovaline). Using CD and NMR techniques we were able to show that both heptapeptides are well structured in water, and that the type of conformation adopted is indeed the ternary 310-helix.
N-acetonylbenzamide fungicides
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, (2008/06/13)
This invention relates to new compositions comprising predominantly one enantiomer of an N-acetonylbenzamide fungicide, methods of preparing N-acetonylbenzamides, and their use as fungicides.
