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Catalog Number:
03141
CAS Number:
17114-97-5
Chlorhydrate d'ester méthylique d'O- tert -butyl-L-sérine
Purity:
97,5 - 102,5 % (dosage par titrage)
Synonym(s):
Chlorhydrate d'ester méthylique d'O-tert-butyl-L-sérine
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Product Information

O-tert-Butyl-L-serine methyl ester hydrochloride is a versatile compound widely utilized in the fields of pharmaceuticals and biochemistry. This compound serves as a valuable building block in the synthesis of various bioactive molecules, particularly in the development of peptide-based therapeutics. Its unique tert-butyl protecting group enhances stability and solubility, making it an ideal candidate for researchers focused on drug formulation and delivery systems.

In addition to its applications in medicinal chemistry, O-tert-Butyl-L-serine methyl ester hydrochloride is also employed in the synthesis of chiral intermediates, which are crucial for the production of enantiomerically pure compounds. This compound's ability to facilitate asymmetric synthesis positions it as a key player in the development of novel pharmaceuticals, agrochemicals, and fine chemicals. With its favorable properties and practical applications, O-tert-Butyl-L-serine methyl ester hydrochloride is an essential tool for researchers and industry professionals aiming to innovate in their respective fields.

Synonyms
Chlorhydrate d'ester méthylique d'O-tert-butyl-L-sérine
CAS Number
17114-97-5
Purity
97,5 - 102,5 % (dosage par titrage)
Molecular Formula
C8H17NO3 · HCl
Molecular Weight
211.7
MDL Number
MFCD00077108
PubChem ID
44181879
Melting Point
157 - 167 °C
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = 8,0 ± 1,5 º (C = 1 dans CH 3 OH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Chlorhydrate d'ester méthylique d'O-tert-butyl-L-sérine
CAS Number
17114-97-5
Purity
97,5 - 102,5 % (dosage par titrage)
Molecular Formula
C8H17NO3 · HCl
Molecular Weight
211.7
MDL Number
MFCD00077108
PubChem ID
44181879
Melting Point
157 - 167 °C
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = 8,0 ± 1,5 º (C = 1 dans CH 3 OH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

O-tert-Butyl-L-serine methyl ester hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, which are essential in drug development and biochemistry.
  • Pharmaceutical Applications: It is used in the formulation of various pharmaceutical compounds, enhancing solubility and bioavailability, making medications more effective.
  • Bioconjugation: The compound plays a crucial role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital in diagnostics and therapeutic applications.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter functions, aiding in the understanding of neurological disorders and potential treatments.
  • Protein Engineering: This chemical is utilized in protein engineering to modify amino acid sequences, which can lead to the development of proteins with enhanced properties for industrial or medical use.

Citations