123444-68-8 Usage
Description
(3S)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is a chiral chemical compound that belongs to the class of organic compounds known as alpha-hydroxyaldehydes. It contains a silanol group and a butanal group, and its molecular formula is C20H28O2Si with a molecular weight of 328.53 g/mol. (3S)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is characterized by its unique three-dimensional structure, which may contribute to its potential applications in various chemical and pharmaceutical industries.
Uses
Used in Chemical Synthesis:
(3S)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is used as a key intermediate in the synthesis of various complex organic molecules. Its unique structure and reactivity make it a valuable building block for creating novel compounds with specific properties and functions.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, (3S)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal may be utilized as a chiral auxiliary or a precursor in the development of new drugs. Its distinct stereochemistry can be exploited to control the stereoselectivity of chemical reactions, leading to the production of enantiomerically pure pharmaceutical compounds.
Used in Material Science:
(3S)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal's silanol group may also find applications in material science, particularly in the development of new materials with specific properties. For instance, it could be used in the synthesis of silane-based polymers or as a component in the creation of self-assembling materials.
Check Digit Verification of cas no
The CAS Registry Mumber 123444-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,4 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 123444-68:
(8*1)+(7*2)+(6*3)+(5*4)+(4*4)+(3*4)+(2*6)+(1*8)=108
108 % 10 = 8
So 123444-68-8 is a valid CAS Registry Number.
123444-68-8Relevant articles and documents
Stereoselective Total Synthesis of Carolacton
Kuilya, Tapan Kumar,Goswami, Rajib Kumar
, p. 2366 - 2369 (2017)
A short and convergent strategy for the stereoselective total synthesis of biologically active natural product carolacton has been accomplished. Our synthesis highlights the Urpi acetal aldol, Crimmins aldol, Ireland-Claisen rearrangement, TiCl4/sub
Asymmetric Total Synthesis of Mycobacterial Diacyl Trehaloses Demonstrates a Role for Lipid Structure in Immunogenicity
Holzheimer, Mira,Reijneveld, Josephine F.,Ramnarine, Alexandrea K.,Misiakos, Georgios,Young, David C.,Ishikawa, Eri,Cheng, Tan-Yun,Yamasaki, Sho,Moody, D. Branch,Van Rhijn, Ildiko,Minnaard, Adriaan J.
, p. 1835 - 1841 (2020/08/26)
The first asymmetric total synthesis of three structures proposed for mycobacterial diacyl trehaloses, DAT1, DAT2, and DAT3 is reported. The presence of two of these glycolipids, DAT1 and DAT3, within different strains of pathogenic M. tuberculosis was co
Synthesis of stereopure acyclic 1,5-dimethylalkane chirons: Building blocks of highly methyl-branched natural products
Li, Nan-Sheng,Piccirilli, Joseph A.
, p. 9633 - 9641 (2013/10/22)
An efficient synthetic method towards stereopure acyclic 1,5-dimethylalkane building blocks from methyl (2R)-3-hydroxy-2-methylpropionate (R)-1 (>99% ee) and methyl (2S)-3-hydroxy-2-methylpropionate (S)-1 (>99% ee) through a series of chemical transformat
