Methyl azetidine-3-carboxylate hydrochloride - CAS 100202-39-9

Methyl azetidine-3-carboxylate hydrochloride - CAS 100202-39-9 Catalog number: BADC-01915

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Methyl azetidine-3-carboxylate hydrochloride is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Category
ADCs Linker
Product Name
Methyl azetidine-3-carboxylate hydrochloride
CAS
100202-39-9
Catalog Number
BADC-01915
Molecular Formula
C5H10ClNO2
Molecular Weight
151.59
Purity
>97%
Methyl azetidine-3-carboxylate hydrochloride

Ordering Information

Catalog Number Size Price Quantity
BADC-01915 -- $-- Inquiry
Description
Methyl azetidine-3-carboxylate hydrochloride is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Synonyms
Azetidine-3-carboxylic acid methyl ester hydrochloride; 3-Azetidinecarboxylic acid, methyl ester, hydrochloride (1:1)
IUPAC Name
methyl azetidine-3-carboxylate;hydrochloride
Canonical SMILES
COC(=O)C1CNC1.Cl
InChI
InChI=1S/C5H9NO2.ClH/c1-8-5(7)4-2-6-3-4;/h4,6H,2-3H2,1H3;1H
InChIKey
UOCWTLBPYROHEF-UHFFFAOYSA-N
Melting Point
93-97°C
Boiling Point
187-192°C at 760 mmHg

Methyl azetidine-3-carboxylate hydrochloride, a versatile compound used in diverse scientific research and industrial applications, boasts a wide range of uses.

Pharmaceutical Research: A cornerstone of pharmaceutical research, methyl azetidine-3-carboxylate hydrochloride plays a pivotal role as a foundational building block for synthesizing cutting-edge drug candidates. Its intricate structure lends itself to a myriad of chemical modifications, facilitating the creation of compounds with enhanced pharmacological properties. Researchers harness the potential of this compound to explore novel therapeutic agents targeting a multitude of diseases.

Chemical Synthesis: Embedded within the realm of organic synthesis, methyl azetidine-3-carboxylate hydrochloride serves as a vital intermediate in constructing complex molecular architectures. The azetidine ring system it harbors can be seamlessly integrated into diverse chemical frameworks, yielding a broad spectrum of functionalized compounds.

Material Science: Delving into material science, this compound finds its niche in the development of polymers and cutting-edge materials. The incorporation of the azetidine moiety imparts distinctive mechanical and thermal properties to polymeric materials, enabling the design of materials tailored for specific applications such as coatings, adhesives, and high-performance composites.

Biochemical Studies: Within the realm of biochemical research, methyl azetidine-3-carboxylate hydrochloride emerges as a powerful tool for investigating enzyme interactions and unraveling biochemical pathways. Its structural characteristics position it as a versatile probe in enzyme-substrate studies, shedding light on enzyme specificity and catalytic mechanisms.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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