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73711-65-6

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73711-65-6 Usage

Description

((4R,5R)-5-(hydroxyMethyl)-2,2-diMethyl-1,3-dioxolan-4-yl)Methyl 4-Methylbenzenesulfonate is a sulfonate ester that contains a dioxolane ring and a benzene ring. It has a molecular formula C16H24O5S and a molecular weight of 328.42 g/mol. This colorless to light yellow liquid is known for its stability under normal temperatures and pressures.
Used in Organic Synthesis:
((4R,5R)-5-(hydroxyMethyl)-2,2-diMethyl-1,3-dioxolan-4-yl)Methyl 4-Methylbenzenesulfonate is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions and contribute to the formation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ((4R,5R)-5-(hydroxyMethyl)-2,2-diMethyl-1,3-dioxolan-4-yl)Methyl 4-Methylbenzenesulfonate is used as a key intermediate in the synthesis of certain drugs, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
((4R,5R)-5-(hydroxyMethyl)-2,2-diMethyl-1,3-dioxolan-4-yl)Methyl 4-Methylbenzenesulfonate is also utilized in the agrochemical industry, where it serves as a component in the production of various agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 73711-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,1 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73711-65:
(7*7)+(6*3)+(5*7)+(4*1)+(3*1)+(2*6)+(1*5)=126
126 % 10 = 6
So 73711-65-6 is a valid CAS Registry Number.

73711-65-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S)-2,3-(propane-2,2-dioxy)-4-hydroxy-1-butyl p-toluenesulfonate

1.2 Other means of identification

Product number -
Other names (2S,3S)-1-O-p-toluenesulfonyl-2,3-O-isopropylidene-L-threitol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73711-65-6 SDS

73711-65-6Relevant articles and documents

MACROCYCLIC COMPOUNDS AND THEIR USE IN THE TREATMENT OF DISEASE

-

Page/Page column 63; 64, (2020/07/14)

The invention relates to heterocyclic compounds of the formula (I), in which all of the variables are as defined in the specification; capable of modulating the activity of CFTR. The invention further provides a method for manufacturing compounds of the invention, and its therapeutic uses. The invention further provides methods to their preparation, to their medical use, in particular to their use in the treatment and management of diseases or disorders including Cystic fibrosis and related disorders.

Rapid and scalable synthesis of chiral bromolactones as precursors to α-exo-methylene-γ-butyrolactone-containing sesquiterpene lactones

Lagoutte, Roman,Pastor, Miryam,Berthet, Mathéo,Winssinger, Nicolas

supporting information, p. 6012 - 6021 (2018/09/11)

The sesquiterpene lactones cover a diverse and pharmacologically important diversity space. In particular, the electrophilic α-exo-methylene-γ-butyrolactone moiety that is preponderant in this natural product family has been shown to readily engage in cov

Synthesis of diacylglycerol analogs bearing photoaffinity tags for labelling mammalian diacylglycerol kinase

Eni, Sammy Eni,Rowland, Meng,Best, Michael D.

, p. 25457 - 25461 (2015/03/30)

Signaling lipids such as diacylglycerol (DAG), phosphatidic acid, and the phosphatidylinositol polyphosphates are site-specific ligands for protein binding partners. Herein, we report the apotheoses of our initial approach to the development of diverse probes which are vital for understanding lipid-protein interactions. When incorporated into liposomes, these probes reduce mammalian diacylglycerol kinase's (DGK) enzymatic activity in a concentration, time, and light dependent manner. This journal is

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