CAS 82962-54-7

2,2-Dimethyl-5-ethoxycarbonyl-1,3-dioxane

Description:

2,2-Dimethyl-5-ethoxycarbonyl-1,3-dioxane, with the CAS number 82962-54-7, is an organic compound characterized by its dioxane ring structure, which features two ether linkages and a carbonyl group. This compound typically exhibits a colorless to pale yellow appearance and is soluble in organic solvents, making it useful in various chemical applications. The presence of the ethoxycarbonyl group contributes to its reactivity, particularly in esterification and acylation reactions. The dimethyl substituents on the dioxane ring enhance its steric hindrance, which can influence its reactivity and interactions with other molecules. Additionally, the compound may exhibit moderate stability under standard conditions but should be handled with care due to potential reactivity with strong nucleophiles or bases. Its unique structure and functional groups make it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. As with all chemical substances, proper safety measures should be observed when handling this compound.

Synonyms:

• 2,2-diMethyl-5-ethoxycarbonyl-1,3-dioxane
• Methyl 2,2-diMethyl-1,3-dioxane-5-carboxylate
• 2,2-Dimethyl-[1,3]dioxane-5-carboxylic acid ethyl ester
• ethyl 2,2-diMethyl-1,3-dioxane-5-carboxylate
• 1,3-Dioxane-5-carboxylic acid, 2,2-dimethyl-, ethyl ester

2,2-diMethyl-5-ethoxycarbonyl-1,3-dioxane

CAS: 82962-54-7

Formula: C₉H₁₆O₄

Purity: 95%

Color and Shape: Liquid

Molecular weight: 188.2209

Ref: IN-DA00G42H

2,2-Dimethyl-5-carbethoxy-1,3-dioxane

CAS: 82962-54-7

2,2-Dimethyl-5-carbethoxy-1,3-dioxane

Purity: 95%

Molecular weight: 188.22g/mol

Ref: 54-OR74604

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate

CAS: 82962-54-7

Formula: C₉H₁₆O₄

Purity: 96%

Color and Shape: Liquid

Molecular weight: 188.223

Ref: 10-F321475

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate

CAS: 82962-54-7

Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate is a nucleoside phosphonate that is used in the synthesis of nucleotides and nucleosides. Ethyl 2,2-dimethyl-1,3-dioxane-5-carboxylate inhibits viral replication by binding to the purine base in DNA and RNA. This compound has been shown to be effective against adefovir resistant strains of human immunodeficiency virus (HIV). It also inhibits the synthesis of pyrimidine nucleotides and uracil nucleosides, which are important for viral replication.

Formula: C₉H₁₆O₄

Purity: Min. 95%

Molecular weight: 188.22 g/mol

Ref: 3D-FE154173