143140-08-3 Usage
General Description
(S)-(-)-N-METHOXYMETHYL-N-(TRIMETHYLSILYL)METHYL-1-PHENYLETHYLAMINE is a chemical compound that belongs to the class of organic compounds known as diphenylmethanes. It is a chiral compound with a specific stereochemistry, denoted by the (S)-(-) designation. (S)-(-)-N-METHOXYMETHYL-N-(TRIMETHYLSILYL)METHYL-1-PHENYLETHYLAMINE contains a methoxy group, a trimethylsilyl group, a methyl group, and a phenylethylamine group, all of which are important functional groups that can impart specific properties to the compound. (S)-(-)-N-METHOXYMETHYL-N-(TRIMETHYLSILYL)METHYL-1-PHENYLETHYLAMINE may have potential applications in organic synthesis, pharmaceuticals, or materials science due to its unique structure and properties. It is important to handle and use this compound with care, following proper safety protocols and regulations.
Check Digit Verification of cas no
The CAS Registry Mumber 143140-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,1,4 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143140-08:
(8*1)+(7*4)+(6*3)+(5*1)+(4*4)+(3*0)+(2*0)+(1*8)=83
83 % 10 = 3
So 143140-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H25NOSi/c1-13(14-9-7-6-8-10-14)15(11-16-2)12-17(3,4)5/h6-10,13H,11-12H2,1-5H3/t13-/m0/s1
143140-08-3Relevant articles and documents
HETEROCYCLIC COMPOUNDS FOR MEDIATING TYROSINE KINASE 2 ACTIVITY
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, (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.
