39986-37-3 Usage
Description
2,4-DIMETHYL-4-HYDROXYMETHYL-2-OXAZOLINE is a heterocyclic chemical compound characterized by a molecular formula of C6H11NO2. It features a 5-membered oxazoline ring with two methyl groups and a hydroxymethyl group attached, making it a versatile building block in the synthesis of pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
2,4-DIMETHYL-4-HYDROXYMETHYL-2-OXAZOLINE serves as a precursor in the synthesis of various pharmaceuticals, contributing to the development of new drugs. Its unique structure allows for the introduction of the oxazoline moiety into different molecules, enhancing their therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-DIMETHYL-4-HYDROXYMETHYL-2-OXAZOLINE is utilized as a precursor for the synthesis of agrochemicals, playing a crucial role in the development of effective and environmentally friendly products.
Used as a Reagent in Organic Synthesis:
2,4-DIMETHYL-4-HYDROXYMETHYL-2-OXAZOLINE is employed as a reagent in organic synthesis to introduce the oxazoline moiety into different molecules. This allows for the creation of new compounds with potential applications in various fields.
Used in Biological Activity Research:
2,4-DIMETHYL-4-HYDROXYMETHYL-2-OXAZOLINE has been studied for its potential biological activity, which may contribute to the discovery of new drugs and therapeutic agents. Its unique structure and properties make it a promising candidate for further research and development in the pharmaceutical and agrochemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 39986-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,8 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39986-37:
(7*3)+(6*9)+(5*9)+(4*8)+(3*6)+(2*3)+(1*7)=183
183 % 10 = 3
So 39986-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c1-5-7-6(2,3-8)4-9-5/h8H,3-4H2,1-2H3
39986-37-3Relevant articles and documents
Catalytic conversion of glycerol to allyl alcohol; Effect of a sacrificial reductant on the product yield
Sanchez, Gizelle,Friggieri, Jarrod,Adesina, Adesoji A.,Dlugogorski, Bogdan Z.,Kennedy, Eric M.,Stockenhuber, Michael
, p. 3090 - 3098 (2014/08/18)
A continuous process for the conversion of glycerol to allyl alcohol, where ammonia or organic acids are added to the feed as sacrificial reductants, was investigated. Significant enhancement on the rate of formation and yield of the allyl alcohol is observed with some of the reducing agents examined over an alumina-supported iron catalyst. Optimising the molar ratio of the reductant relative to feed glycerol results in an increase in the yield of allyl alcohol from 9% (in the absence of additives) to 11.3% with ammonia, 15.1% with ammonium hydroxide, 17.8% with oxalic acid and 19.5% with formic acid. Moreover, the addition of other organic acids, which are produced in a typical glycerol conversion experiment, was studied. However, acetic and propanoic acids had little effect on the rate of formation of allyl alcohol. Analysis of the product distribution in the liquid and gas phases when oxalic and formic acids were added suggests a two-step process for the formation of allyl alcohol under the operating conditions of the reaction; the initial step involves the dehydration of glycerol while the second comprises the reduction of the species produced in step one. the Partner Organisations 2014.
