CAS 429669-07-8

1-Azetidinecarboxylicacid, 3-methoxy-, 1,1-dimethylethyl ester

Description:

1-Azetidinecarboxylic acid, 3-methoxy-, 1,1-dimethylethyl ester, identified by CAS number 429669-07-8, is an organic compound characterized by its azetidine ring structure, which is a four-membered cyclic amine. This compound features a carboxylic acid functional group, which is esterified with a tert-butyl group, enhancing its stability and lipophilicity. The presence of a methoxy group at the 3-position of the azetidine ring contributes to its chemical reactivity and potential biological activity. Generally, compounds of this nature may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The molecular structure suggests potential applications in drug development, particularly in areas requiring compounds with specific stereochemical configurations. Additionally, the presence of both the methoxy and tert-butyl groups may influence the compound's solubility and interaction with biological targets. As with many organic compounds, the specific characteristics such as melting point, boiling point, and solubility would depend on the molecular interactions and the environment in which the compound is studied.

Formula: C₉H₁₇NO₃

Synonyms:

• tert-Butyl 3-methoxyazetidine-1-carboxylate
• 1-Boc-3-(Methoxy)Azetidine
• N-Boc-3-Methoxyazetidine

1-Boc-3-(methoxy)azetidine

CAS: 429669-07-8

Formula: C₉H₁₇NO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 187.2362

Ref: IN-DA00BXWW

3-Methoxyazetidine, N-BOC protected

CAS: 429669-07-8

3-Methoxyazetidine, N-BOC protected

Purity: 98%

Molecular weight: 187.24g/mol

Ref: 54-OR40390

1-Boc-3-(methoxy)azetidine

CAS: 429669-07-8

Formula: C₉H₁₇NO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 187.239

Ref: 10-F217989

1-Boc-3-(methoxy)azetidine

CAS: 429669-07-8

1-Boc-3-(methoxy)azetidine is an allylated azetidine that is used in the synthesis of heterocyclic compounds. It has been found to be a useful electrophile for the stereoselective synthesis of certain carbonyl derivatives, such as cyclopropane, benzaldehyde, and cyclopentanol.
The 1-Boc-3-(methoxy)azetidine is synthesized by reacting ethyl bromoacetate with 3-methyl-2-oxazolidinone. The intermediate product is then reduced with lithium aluminum hydride, followed by the addition of methoxylamine hydrochloride to give the desired product.

Formula: C₉H₁₇NO₃

Purity: Min. 95%

Molecular weight: 187.24 g/mol

Ref: 3D-ESA66907