1-Boc-azetidine-3-yl-methanol - CAS 142253-56-3

1-Boc-azetidine-3-yl-methanol - CAS 142253-56-3 Catalog number: BADC-01645

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1-Boc-azetidine-3-yl-methanol is a non-cleavable ADC linker and also an alkyl chain-based PROTAC linker.

Category
ADCs Linker
Product Name
1-Boc-azetidine-3-yl-methanol
CAS
142253-56-3
Catalog Number
BADC-01645
Molecular Formula
C9H17NO3
Molecular Weight
187.24
1-Boc-azetidine-3-yl-methanol

Ordering Information

Catalog Number Size Price Quantity
BADC-01645 -- $--
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Description
1-Boc-azetidine-3-yl-methanol is a non-cleavable ADC linker and also an alkyl chain-based PROTAC linker.
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
LogP
0.78350
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

Historical Records: 1-Boc-azetidine-3-yl-methanol
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