10340-88-2 Usage
Uses
Used in Chemical Synthesis:
1,2-Dimethoxyethylene is used as a solvent in chemical reactions for its ability to dissolve a wide range of substances and facilitate various chemical processes.
Used in Pharmaceutical Production:
1,2-Dimethoxyethylene is used as a precursor in the production of pharmaceuticals, contributing to the synthesis of various medicinal compounds.
Used in Adhesive Formulation:
1,2-Dimethoxyethylene is used as a component in the formulation of adhesives, enhancing their performance and bonding capabilities.
Used in Coating Formulation:
1,2-Dimethoxyethylene is used in the formulation of coatings, improving their properties such as adhesion, flexibility, and durability.
Used in Specialty Chemicals:
1,2-Dimethoxyethylene is used as a component in the development of specialty chemicals, where its unique properties are leveraged for specific applications.
Safety Precautions:
Due to its flammability and potential for harmful effects if inhaled or ingested, 1,2-dimethoxyethylene should be handled with caution, using appropriate safety measures and equipment.
Check Digit Verification of cas no
The CAS Registry Mumber 10340-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10340-88:
(7*1)+(6*0)+(5*3)+(4*4)+(3*0)+(2*8)+(1*8)=62
62 % 10 = 2
So 10340-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O2/c1-5-3-4-6-2/h3-4H,1-2H3/b4-3+
10340-88-2Relevant academic research and scientific papers
Tilborg, M. W. E. M. van,Doorn, R. van,Nibbering, N. M. M.
, p. 152 - 156 (1980)
The ion/molecule reactions of allyl cations and 2-methoxyallyl cations with vinyl methyl ether, 1-chloro-2-ethoxyethene and 1,2-dimethoxyethene are discussed in terms of cycloaddition reactions.Deuterium labelling of the cations has been used for the study of the reaction mechanisms.The appearance of various product ions in these ion/molecule reactions lead to the suggestion that in reactions of allyl cations with alkenes non-cyclic + product ions are formed preferentially, but that in reactions of 2-methoxyallyl cations with alkenes a significant part of the product ions are methoxycyclopentadienyl cations.These observations are ascribed to the stabilizing effect of the methoxy group with regard to the positive charge in the product ions.
