webinar
Oct. 27-28, 2025, Boston, MA, USA - Booth 114.
Read More

1-Boc-azetidine-3-yl-methanol

  CAS No.: 142253-56-3   Cat No.: BADC-01645 4.5  

1-Boc-azetidine-3-yl-methanol serves as a cyclic linker intermediate in ADC synthesis, facilitating stable antibody conjugation with enhanced targeting and payload delivery capabilities.

1-Boc-azetidine-3-yl-methanol

Structure of 142253-56-3

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C9H17NO3
Molecular Weight
187.24

* For research and manufacturing use only. We do not sell to patients.

Size Price Stock Quantity
-- $-- In stock

Looking for different specifications? Click to request a custom quote!

Capabilities & Facilities

Popular Publications Citing BOC Sciences Products
Synonyms
1-Boc-azetidine-3-ylmethanol; 3-hydroxymethylazetidine-1-carboxylic acid tert-butyl ester
IUPAC Name
tert-butyl 3-(hydroxymethyl)azetidine-1-carboxylate
Canonical SMILES
CC(C)(C)OC(=O)N1CC(C1)CO
InChI
InChI=1S/C9H17NO3/c1-9(2,3)13-8(12)10-4-7(5-10)6-11/h7,11H,4-6H2,1-3H3
InChIKey
HXRDRJKAEYHOBB-UHFFFAOYSA-N
Density
1.115 g/cm3
Melting Point
55°C
Appearance
White to Off-white Solid
Signal Word
Warning
Boiling Point
268-273°C at 760 mmHg

1-Boc-azetidine-3-yl-methanol, a pivotal intermediate in organic synthesis, plays a crucial role in the intricate world of complex pharmaceutical development. Here are four key applications presented with high perplexity and burstiness:

Custom Synthesis: Widely embraced in custom synthesis, 1-Boc-azetidine-3-yl-methanol stands out as a foundational element for constructing intricate organic molecules. Its unique structural design acts as a cornerstone in synthesizing diverse pharmacologically active compounds. Chemists harness its reactivity to forge novel bonds, enabling the inception of elaborate molecular architectures.

Pharmaceutical Development: Positioned at the forefront of pharmaceutical innovation, 1-Boc-azetidine-3-yl-methanol acts as a pivotal precursor for synthesizing potential drug candidates. Its significance lies in shaping small molecules vital for medicinal chemistry endeavors targeting a spectrum of ailments. This compound plays a vital role in sculpting precise molecular structures essential for the intended biological efficacy of novel therapeutic agents.

Chemical Research: Enterprising researchers turn to 1-Boc-azetidine-3-yl-methanol in their quest to delve into uncharted chemical territories and pathways. Its versatile chemical attributes render it an ideal subject for unraveling reaction mechanisms and pioneering synthetic methodologies. By harnessing this compound, scientists can unearth novel transformations and refine synthetic pathways, pushing the boundaries of chemical exploration.

Material Science: While primarily associated with pharmaceutical synthesis, 1-Boc-azetidine-3-yl-methanol ventures into the realm of material science, expanding its reach into the preparation of cutting-edge materials like polymers and specialty chemicals. Its integration into polymer structures can yield materials endowed with distinctive properties suitable for a myriad of high-performance applications.

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

Related Products

Contact our experts today for pricing and comprehensive details on our ADC offerings.

You May Also Be Interested In

From cytotoxin synthesis to linker design, discover our specialized services that complement your ADC projects.

ADC Linker Development Enzyme Cleavable Linker Cathepsin B Cleavable Linker/Peptide Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker Sulfatase Cleavable Linker Chemically Cleavable Linker Non-Cleavable Linker Services Acid Cleavable Linker/Hydrazone Linker

Unlock Deeper ADC Insights

Learn more about payload design, linker strategies, and integrated CDMO support through our curated ADC content.

Linkers - A Crucial Factor in Antibody–Drug Conjugates In-Depth Review of ADC Linkers: Types, Mechanisms, and Research Progress New Structural Insights Solve Instability Issues of Maleimide Linkers in ADCs PEG Linkers in Antibody-Drug Conjugates Peptide Linkers in Antibody-Drug Conjugates Disulfide Linkers in Antibody-Drug Conjugates Biotinylation Reagents in Antibody-Drug Conjugates Maleimide Linkers in Antibody-Drug Conjugates Current ADC Linker Chemistry SPDB Linkers in Antibody-Drug Conjugates

Explore More ADC Products

Find exactly what your project needs from our expanded range of ADCs, offering flexible options to fit your timelines and goals.

ADC Cytotoxin

Powerful Targeted Cancer Solutions

ADC  Cytotoxin with Linker

Enhanced Stability And Efficacy

ADC Linker

Precise Conjugation For Success

Antibody-Drug  Conjugates (ADCs)

Maximized Therapeutic Performance

Auristatins

Next-Level Tubulin Inhibition

Calicheamicins

High-Impact DNA Targeting

Camptothecins

Advanced Topoisomerase Inhibition

Daunorubicins / Doxorubicins

Trusted Anthracycline Payloads

Duocarmycins

Potent DNA Alkylation Agents

Maytansinoids

Superior Microtubule Disruption

Pyrrolobenzodiazepines

Ultra-Potent DNA Crosslinkers

Traditional Cytotoxic Agents

Proven Chemotherapy Solutions

Cleavable Linker

Precise Intracellular Drug Release

Non-Cleavable Linker

Exceptional Long-Term Stability

Historical Records: DBCO-SS-amine | DBCO-SS-aldehyde | Taltobulin hydrochloride | Daunorubicin | Biotin-PEG3-aldehyde | DBCO-SS-PEG4-Biotin | (+)-CBI-CDPI1 | Kdo Azide | 6-O-Propynyl-2'-deoxyguanosine | bisSP1 | 1-Boc-azetidine-3-yl-methanol
Send Inquiry
Verification code
Inquiry Basket