162698-26-2

Usage

Uses

Used in Pharmaceutical Industry:
Methyl 2-azetidinecarboxylate hydrochloride is used as a precursor in the synthesis of various biologically active compounds for the development of pharmaceuticals. Its unique structure and reactivity make it an important intermediate in the production of valuable chemical products in this industry.
Used in Agrochemical Industry:
In the agrochemical industry, Methyl 2-azetidinecarboxylate hydrochloride is utilized as a building block for the synthesis of agrochemicals, contributing to the development of effective and innovative products for agricultural applications.
Used in Fine Chemicals Production:
Methyl 2-azetidinecarboxylate hydrochloride is also used in the preparation of other fine chemicals, where its versatile properties allow for the creation of a wide range of chemical products with specific applications.
Safety Note:
It is important to handle Methyl 2-azetidinecarboxylate hydrochloride with proper care, as it is classified as a hazardous chemical. Appropriate safety measures should be taken during its use to ensure the well-being of individuals and the environment.

Upstream product

• 255882-95-2 (2S)-Methyl-1-azetidine-2-carboxylic acid 
• 67-56-1 methanol 
• 2517-04-6 Azetidine-2-carboxylic acid 

Downstream Products

• 104587-62-4 azetidin-2-ylmethanol 

Relevant academic research and scientific papers

Carbonyl azetidine substituted naphthalimide fluorescent dye as well as synthesis method and application thereof

The invention provides a novel carbonyl azetidine substituted naphthalimide fluorescent dye as well as synthesis and application thereof. The dye takes 1, 8-naphthalimide as a fluorophore parent, and the fourth site of the 1, 8-naphthalimide is covalently connected with carbonyl azetidine. The novel fluorescent dye has excellent fluorescence intensity and light stability, so that the novel fluorescent dye has wide application prospects in the fields of fluorescence detection, fluorescence imaging and the like, especially in the emerging fields of single molecule detection, super-resolution fluorescence imaging and the like. R1 is H, C1-4 alkyl and aryl, R2 is shown in the specification, and in R2, X1 is H, C1-2 alkyl, X2 is C1-2 alkyl or shown in the specification, X3 is C1-2 alkyl or shown in the specification, and X4 is C1-2 alkyl.

Carbonyl azetidine substituted coumarin fluorescent dye as well as synthesis method and application thereof

The invention provides a novel carbonyl azetidine substituted coumarin fluorescent dye as well as synthesis and application thereof. The structural innovation of the dye is that carbonyl azetidine is covalently linked to the No.7 site of a coumarin parent. The novel fluorescent dye has excellent fluorescence intensity and light stability, so that the novel fluorescent dye has wide application prospects in the fields of fluorescence detection, fluorescence imaging and the like, especially in the emerging fields of single molecule detection, super-resolution fluorescence imaging and the like. R1 is C1-4 alkyl, and R2 is shown in the specification, X1 is H or C1-2 alkyl, X2 is C1-2 alkyl or shown in the specification, X3 is C1-2 alkyl or shown in the specification, and X4 is C1-2 alkyl.

Carbonyl azetidine substituted NBD fluorescent dye as well as synthesis method and application thereof

The invention provides a novel carbonyl azetidine substituted NBD fluorescent dye as well as synthesis and application thereof. The structure of the dye is characterized in that carbonyl azetidine is covalently connected to the fourth site of a 4-chloro-7-nitrobenzene-2-oxa-1, 3-diazole (NBD) parent. The novel fluorescent dye has excellent fluorescence intensity and light stability, so that the novel fluorescent dye has wide application prospects in the fields of fluorescence detection, fluorescence imaging and the like, especially in the emerging fields of single molecule detection, super-resolution fluorescence imaging and the like. R1 is as described in the specification, X1 is H or C1-2 alkyl, X2 is C1-2 alkyl or as described in the specification, x3 is C1-2 alkyl or as described in the specification, and X4 is C1-2 alkyl.

Neurotrophic 2-azetidinecarboxylic acid derivatives, and related compositions and methods

This invention provides compounds having the following general structure: This invention also provides pharmaceutical compositions comprising same and methods of using these compositions to treat and prevent disorders characterized by neuronal damage.