135782-16-0 Usage
Description
(S)-1-Phenyl-N-((trimethylsilyl)methyl)ethanamine, with the molecular formula C12H19NSi, is a chiral amine characterized by the presence of a phenyl group and a trimethylsilylmethyl group attached to the nitrogen atom. (S)-1-Phenyl-N-((trimethylsilyl)methyl)ethanamine is known for its stability and ease of handling in chemical reactions, largely due to the protective trimethylsilyl group.
Uses
Used in Pharmaceutical Synthesis:
(S)-1-Phenyl-N-((trimethylsilyl)methyl)ethanamine is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure and properties make it a valuable component in the creation of complex molecular structures.
Used in Agrochemical Production:
In the agrochemical industry, (S)-1-Phenyl-N-((trimethylsilyl)methyl)ethanamine serves as an intermediate for the synthesis of various agrochemicals, including pesticides and other compounds that aid in crop protection and enhancement.
Used in Organic Chemistry:
(S)-1-Phenyl-N-((trimethylsilyl)methyl)ethanamine is also utilized as a reagent in the preparation of chiral amine derivatives, which are essential in organic chemistry for the synthesis of a wide range of compounds with specific stereochemistry.
Used in Chemical Research:
(S)-1-Phenyl-N-((trimethylsilyl)methyl)ethanamine is a valuable building block for researchers in the field of organic chemistry, as it allows for the exploration of new synthetic pathways and the development of novel chemical methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 135782-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,8 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135782-16:
(8*1)+(7*3)+(6*5)+(5*7)+(4*8)+(3*2)+(2*1)+(1*6)=140
140 % 10 = 0
So 135782-16-0 is a valid CAS Registry Number.
135782-16-0Relevant articles and documents
HETEROCYCLIC COMPOUNDS FOR MEDIATING TYROSINE KINASE 2 ACTIVITY
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Page/Page column 90, (2021/01/23)
Heterocyclic compounds shown in Formula (I) suitable for inhibiting or regulating the activity of Janus kinase (JAK), particularly tyrosine kinase 2 (TYK2). The compounds are useful for preventing and/or treating relevant JAK-mediated diseases, such as autoimmune diseases, inflammatory diseases, and cancers.
QUINOLONE ANTIBACTERIAL AGENTS
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Page/Page column 86; 87; 116, (2010/02/12)
Compounds of formula (I) wherein A is formula (II), formula (III) or formula (IV), and B is formula (V), formula (VI), or formula (VII), can be used in a variety of applications including use as antibacterial agents.
Non-stabilized azomethine ylides in [3 + 2] cycloadditions. Pyrrolidinylfuranones from (5S)-5-menthyloxy-4-vinylfuran-2(5H)-one
Gerlach, Kai,Hoffmann,Wartchow
, p. 3867 - 3872 (2007/10/03)
Upon sonication with lithium fluoride in acetonitrile N-benzyl-N-methoxymethyl(trimethylsilylmethyl)amines 9a-c undergo chemoselective 1,3-dipolar cycloaddition with 4-vinylfuranones 2 and 6 to afford pyrrolidinylfuranones 10, 11a-c and 12a-c. The stereochemistry is assigned by X-ray analyses and proton NMR data comparison of related oxiranylfuranone 13.
