14036-06-7 Usage
Description
Diethoxymethyl acetate is a colorless liquid that is known for its ability to react with various compounds, such as 5-amino-6-ribitylaminouracil hydrochloride, to yield 6-dioxo-(1H,3H)-9-N-ribitylpurine. This characteristic makes it a valuable component in the synthesis of different nucleosides.
Uses
Used in Pharmaceutical Synthesis:
Diethoxymethyl acetate is used as a synthetic intermediate for the production of various theophylline nucleosides, such as D-mannosyl, D-galactosyl, and D-glucosyl theophylline nucleosides. These nucleosides are essential in the development of pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Research:
As a colorless liquid with unique reactivity, diethoxymethyl acetate is also utilized in chemical research for the development and study of new compounds and reactions. Its ability to react with specific compounds makes it a valuable tool in the exploration of novel chemical pathways and the creation of new pharmaceutical agents.
Check Digit Verification of cas no
The CAS Registry Mumber 14036-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,3 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14036-06:
(7*1)+(6*4)+(5*0)+(4*3)+(3*6)+(2*0)+(1*6)=67
67 % 10 = 7
So 14036-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O4/c1-4-9-7(10-5-2)11-6(3)8/h7H,4-5H2,1-3H3
14036-06-7Relevant articles and documents
Substitution of the acetoxy groups of dialkoxymethylacetates by organometallic reagents: a route to allyl-, propargyl-, homoallyl-, homopropargyl- and α-stannylacetals
Beaudet, Isabelle,Duchene, Alain,Parrain, Jean-Luc,Quintard, Jean-Paul
, p. 201 - 212 (2007/10/02)
The substitution of the acetoxy groups of dialkoxymethylacetates by organometallic reagents has been examined in a search for new methods of preparing functional acetals.The efficiency of the substitution of the acetoxy group is highly dependent on the nature of the organometallic reagents: soft nucleophiles with strong electrophilic assistance by the counterion are the best reagents.Allyl-, propargyl-, homoallyl-, homopropargyl- and α-stannylacetals have been made by this route, in which dialkoxymethylacetates often function as useful substitutes for dialkylphenylorthoformates.
