N-Carbobenzoxy-β-alaninol
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N-Carbobenzoxy-β-alaninol

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N-Carbobenzoxy-β-alaninol (CAS# 34637-22-4) is a useful research chemical.

Category
Amino Alcohol
Catalog number
BAT-000684
CAS number
34637-22-4
Molecular Formula
C11H15NO3
Molecular Weight
209.24
N-Carbobenzoxy-β-alaninol
Size Price Stock Quantity
100 g $199 In stock
IUPAC Name
benzyl N-(3-hydroxypropyl)carbamate
Synonyms
Z-β-Ala-ol; Z-NH-(CH2)3-OH; 3-(Carbobenzoxyamino)-1-propanol; Benzyl (3-hydroxypropyl)carbamate; Benzyl N-(3-hydroxypropyl)carbamate; 3-(Cbz-amino)-1-propanol
Appearance
White to off-white powder or crystals
Density
1.152 g/cm3
Melting Point
49-51 °C
Boiling Point
392.5 °C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C11H15NO3/c13-8-4-7-12-11(14)15-9-10-5-2-1-3-6-10/h1-3,5-6,13H,4,7-9H2,(H,12,14)
InChI Key
WXQCFKYWSKKNKY-UHFFFAOYSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NCCCO

N-Carbobenzoxy-β-alaninol, a vital chemical compound in bioscience and pharmaceutical industries, finds diverse applications in various fields. Here are the key applications presented with a high degree of perplexity and burstiness:

Peptide Synthesis: Serving as a fundamental building block in peptide synthesis, N-Carbobenzoxy-β-alaninol acts as a safeguarding agent for amino acids preventing premature reactions of the amino group during peptide coupling. This meticulous protection process ensures the efficient production of intricate peptides tailored for both research endeavors and therapeutic pursuits.

Medicinal Chemistry: Embedded in the realm of medicinal chemistry, N-Carbobenzoxy-β-alaninol plays a pivotal role in crafting and synthesizing bioactive compounds. Its adaptable chemistry permits the alteration of peptide structures and the exploration of novel pharmacophores culminating in the unearthing and enhancement of cutting-edge drugs with heightened efficacy and safety profiles.

Organic Synthesis: As a critical intermediary in organic synthesis pathways, N-Carbobenzoxy-β-alaninol's steadfast carbamate protection group proves invaluable in multi-step chemical reactions necessitating precise deprotection measures. This capability empowers chemists in the construction of intricate molecules with unparalleled accuracy and yields pushing the boundaries of organic synthesis methodologies.

Bioconjugation: Unlocking the potential of bioconjugation techniques, N-Carbobenzoxy-β-alaninol facilitates the linking of biomolecules such as proteins and antibodies with other chemical entities. Through strategic modifications introducing functional groups, researchers craft bioconjugates tailored for diagnostic applications drug delivery systems and therapeutic uses broadening the horizons of biomolecule utility in both clinical and research environments.

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