87727-28-4 Usage
Description
(S)-2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-PROPIONALDEHYDE is a unique aldehyde compound characterized by its distinct chemical structure, featuring a silane-based ether linkage. (S)-2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-PROPIONALDEHYDE is known for its versatile applications in various industries due to its specific chemical properties.
Used in Chemical Synthesis:
(S)-2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-PROPIONALDEHYDE is used as a raw material in the synthesis of various organic compounds. Its unique structure allows it to serve as a valuable intermediate in the production of complex organic molecules, contributing to the development of new pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, (S)-2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-PROPIONALDEHYDE is used as a flavoring agent. Its distinct aroma profile makes it suitable for enhancing the taste and smell of food and beverage products, providing a pleasant sensory experience for consumers.
Used in Pharmaceutical Industry:
(S)-2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-PROPIONALDEHYDE is used as a key component in the development of pharmaceuticals. Its unique chemical properties enable it to be incorporated into drug molecules, potentially leading to the creation of new medications with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-PROPIONALDEHYDE is utilized in the synthesis of various agrochemical products. Its application in this field contributes to the development of innovative solutions for crop protection and enhancement of agricultural productivity.
Used in Specialty Chemicals:
(S)-2-(TERT-BUTYL-DIMETHYL-SILANYLOXY)-PROPIONALDEHYDE is also used in the production of specialty chemicals, where its unique properties can be leveraged to create high-value products for specific applications, such as in materials science, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 87727-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,2 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87727-28:
(7*8)+(6*7)+(5*7)+(4*2)+(3*7)+(2*2)+(1*8)=174
174 % 10 = 4
So 87727-28-4 is a valid CAS Registry Number.
87727-28-4Relevant articles and documents
Stereoselective synthesis of the chiral tetrahydropyrane core of swinholides and misakinolides
Hayakawa, Hiroyuki,Iida, Kouki,Miyazawa, Masahiro,Miyashita, Masaaki
, p. 601 - 602 (1999)
Stereoselective synthesis of the optically pure tetrahydropyrane core of swinholides and misakinolide A starting from (S)-methyl lactate is described in which the highly stereoselective intramolecular iodoetherification for construction of the tetrahydropyrane ring and the regioselective ring-opening reaction of an epoxide are involved as key steps.
Butenolide synthesis based upon a contra-electronic addition in a ruthenium-catalyzed Alder ene reaction. Synthesis and absolute configuration of (+)-ancepsenolide
Trost, Barry M.,Müller, Thomas J. J.
, p. 4985 - 4986 (1994)
-
SHP2 INHIBITORS AND USES THEREOF
-
Page/Page column 133; 134, (2021/04/02)
Compounds of Formula 1 as inhibitors of protein tyrosine phosphatase SHP2 are disclosed. The pharmaceutical compositions comprising compounds of Formula 1, methods of synthesis of these compounds, methods of treatment for diseases associated with the aberrant activity of SHP2 such as cancer using these compounds or compositions containing these compounds are also disclosed.
A Unified Strategy for the Asymmetric Synthesis of Highly Substituted 1,2-Amino Alcohols Leading to Highly Substituted Bisoxazoline Ligands
Shrestha, Bijay,Rose, Brennan T.,Olen, Casey L.,Roth, Aaron,Kwong, Adon C.,Wang, Yang,Denmark, Scott E.
, p. 3490 - 3534 (2021/02/16)
A general procedure for the asymmetric synthesis of highly substituted 1,2-amino alcohols in high yield and diastereoselectivity is described that uses organometallic additions of a wide range of nucleophiles to tert-butylsulfinimines as the key step. The addition of organolithium reagents to these imines follows a modified Davis model. The diastereoselectivity for this reaction depends significantly on both the nucleophile and electrophile. These highly substituted 1,2-amino alcohols are used to synthesize stereochemically diverse and structurally novel, polysubstituted 2,2′-methylene(bisoxazoline) ligands in high yields.
