1040390-31-5 Usage
Description
(S)-tert-butyl 3-hydroxypent-4-enoate, also known as (S)-t-butyl 3-hydroxypent-4-enoate, is a chemical compound with the molecular formula C10H18O3. It is a derivative of t-butyl hydroxy ester and is characterized by its clear, colorless liquid form with a fruity odor. (S)-tert-butyl 3-hydroxypent-4-enoate is soluble in organic solvents and is widely recognized for its utility as a building block in organic synthesis.
Uses
Used in Flavor and Fragrance Industry:
(S)-tert-butyl 3-hydroxypent-4-enoate is used as a key ingredient for creating natural and synthetic flavors and fragrances, leveraging its fruity scent to enhance various consumer products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (S)-tert-butyl 3-hydroxypent-4-enoate serves as a precursor in the synthesis of diverse compounds, contributing to the development of new medications and therapeutic agents.
Used as a Chiral Building Block:
(S)-tert-butyl 3-hydroxypent-4-enoate is utilized as a chiral building block in organic chemistry, playing a crucial role in the synthesis of complex molecules and pharmaceutical intermediates, where the stereochemistry of the molecule is essential for biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 1040390-31-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,0,3,9 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1040390-31:
(9*1)+(8*0)+(7*4)+(6*0)+(5*3)+(4*9)+(3*0)+(2*3)+(1*1)=95
95 % 10 = 5
So 1040390-31-5 is a valid CAS Registry Number.
1040390-31-5Relevant articles and documents
A Chiral Building Block for the Stereocontrolled Installation of the 1,3-Diol Motif
Bredenkamp, Angela,Zhu, Zhi-Bin,Kirsch, Stefan F.
, p. 252 - 254 (2016)
A new chiral building block for the direct installation of the 1,3-diol motif is presented. Aldehyde olefination followed by directed reduction allows for the synthesis of both the syn- and the anti-configured diol in a fully stereocontrolled way. The building block was used for the total synthesis of naturally occurring 1,2,4-trihydroxynonadecanes starting from pentadecanal.
A stereocontrolled synthesis of the hydrophobic moiety of rhamnolipids
Menhour, Boudjema,Mayon, Patrick,Plé, Karen,Bouquillon, Sandrine,Dorey, Stéphan,Clément, Christophe,Deleu, Magali,Haudrechy, Arnaud
, p. 1159 - 1161 (2015)
A new approach toward the synthesis of the hydrophobic moiety of rhamnolipid derivatives has been developed, involving two key cross-metatheses and an unusual Mitsunobu reaction. Small structural variations of the side chains should enable a better understanding of the role of the lipid moiety in immunostimulatory and plant defense eliciting properties.
Synthesis of the C1-C13 fragment of biselyngbyaside
Sawant, Pramod,Maier, Martin E.
supporting information; experimental part, p. 3002 - 3004 (2012/01/19)
An advanced intermediate vinyl iodide corresponding to the C1-C13 fragment of the macrolide biselyngbyaside was prepared by a cross-metathesis reaction between vinyl alcohol and -alkene building blocks. The latter fragment, containing two stereocenters, w