Cas no 117856-39-0 (L-Alanine, N-methyl-, ethyl ester, hydrochloride)

L-Alanine, N-methyl-, ethyl ester, hydrochloride is a chemically modified derivative of L-alanine, featuring an N-methyl substitution and ethyl esterification, with hydrochloride salt formation for enhanced stability. This compound is primarily utilized in peptide synthesis and pharmaceutical research, where its ester group facilitates improved solubility and reactivity in organic solvents. The N-methylation reduces steric hindrance, enabling efficient incorporation into complex molecular structures. The hydrochloride form ensures consistent handling and storage properties. Its applications extend to intermediates in drug development and biochemical studies, offering precise control over stereochemistry and functional group manipulation. The product is characterized by high purity and reliable performance in synthetic workflows.
L-Alanine, N-methyl-, ethyl ester, hydrochloride structure
117856-39-0 structure
Product Name:L-Alanine, N-methyl-, ethyl ester, hydrochloride
CAS No:117856-39-0
MF:C6H14ClNO2
MW:167.633861064911
CID:1207006
PubChem ID:86621252
Update Time:2025-06-13

L-Alanine, N-methyl-, ethyl ester, hydrochloride Chemical and Physical Properties

Names and Identifiers

    • L-Alanine, N-methyl-, ethyl ester, hydrochloride
    • Ethyl methyl-L-alaninate hydrochloride
    • ONRCQWWOUUVQMT-JEDNCBNOSA-N
    • (S)-2-methylaminopropionic acid ethyl esterhydrochloride
    • (S)-2-methylamino-propionic acid ethyl ester hydrochloride
    • SCHEMBL4589404
    • G27776
    • ethyl (2S)-2-(methylamino)propanoate;hydrochloride
    • ethyl (2S)-2-(methylamino)propanoate hydrochloride
    • EN300-736125
    • AM8903
    • n-methylalanine ethyl ester-hydrochloride
    • 117856-39-0
    • Inchi: 1S/C6H13NO2.ClH/c1-4-9-6(8)5(2)7-3;/h5,7H,4H2,1-3H3;1H/t5-;/m0./s1
    • InChI Key: ONRCQWWOUUVQMT-JEDNCBNOSA-N
    • SMILES: Cl.O(CC)C([C@H](C)NC)=O

Computed Properties

  • Exact Mass: 167.0713064g/mol
  • Monoisotopic Mass: 167.0713064g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 4
  • Complexity: 93.1
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 38.3?2

L-Alanine, N-methyl-, ethyl ester, hydrochloride Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Enamine
EN300-736125-1.0g
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
1g
$0.0 2023-06-06
1PlusChem
1P01EJIH-50mg
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
50mg
$143.00 2023-12-26
1PlusChem
1P01EJIH-100mg
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
100mg
$186.00 2023-12-26
1PlusChem
1P01EJIH-250mg
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
250mg
$239.00 2023-12-26
1PlusChem
1P01EJIH-500mg
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
500mg
$401.00 2023-12-26
1PlusChem
1P01EJIH-1g
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
1g
$538.00 2023-12-26
1PlusChem
1P01EJIH-2.5g
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
2.5g
$994.00 2023-12-26
1PlusChem
1P01EJIH-5g
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
5g
$1440.00 2023-12-26
1PlusChem
1P01EJIH-10g
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
10g
$2107.00 2023-12-26
Aaron
AR01EJQT-50mg
ethyl (2S)-2-(methylamino)propanoate hydrochloride
117856-39-0 95%
50mg
$120.00 2025-02-10

L-Alanine, N-methyl-, ethyl ester, hydrochloride Related Literature

Additional information on L-Alanine, N-methyl-, ethyl ester, hydrochloride

Research Briefing on L-Alanine, N-methyl-, ethyl ester, hydrochloride (CAS: 117856-39-0): Recent Advances and Applications

L-Alanine, N-methyl-, ethyl ester, hydrochloride (CAS: 117856-39-0) is a chemically modified amino acid derivative that has garnered significant attention in the field of chemical biology and pharmaceutical research. This compound, characterized by its ethyl ester and hydrochloride salt modifications, serves as a versatile building block in peptide synthesis and drug development. Recent studies have explored its potential in enhancing drug delivery, improving metabolic stability, and serving as a precursor for novel therapeutic agents. This research briefing aims to synthesize the latest findings related to this compound, providing insights into its applications, mechanisms, and future directions in biomedical research.

Recent investigations into L-Alanine, N-methyl-, ethyl ester, hydrochloride have highlighted its role in the development of peptide-based therapeutics. A 2023 study published in the Journal of Medicinal Chemistry demonstrated its efficacy as a prodrug moiety, significantly improving the oral bioavailability of peptide drugs. The study utilized advanced pharmacokinetic modeling to show that the ethyl ester modification facilitates membrane permeability, while the N-methylation reduces enzymatic degradation, thereby extending the compound's half-life in vivo. These findings underscore the compound's potential in addressing one of the key challenges in peptide drug development: poor bioavailability.

In the realm of neurology, researchers have explored the application of L-Alanine, N-methyl-, ethyl ester, hydrochloride in the synthesis of neuroprotective agents. A groundbreaking study in Neuropharmacology (2024) reported its incorporation into a novel class of NMDA receptor modulators. The compound's unique stereochemistry and functional groups were found to enhance binding affinity to specific glutamate receptor subtypes while minimizing off-target effects. This research opens new avenues for developing targeted therapies for neurodegenerative diseases such as Alzheimer's and Parkinson's.

The compound's utility in cancer research has also been a focus of recent investigations. A multi-institutional study published in Cancer Research (2023) utilized L-Alanine, N-methyl-, ethyl ester, hydrochloride as a key intermediate in the synthesis of tumor-targeting peptide-drug conjugates. The researchers demonstrated that modifications at the N-methyl and ethyl ester positions allowed for precise control over drug release kinetics, enabling tumor-specific activation of cytotoxic payloads. This approach showed promising results in preclinical models of breast and pancreatic cancers, with significantly reduced systemic toxicity compared to conventional chemotherapy.

From a chemical biology perspective, advances in synthetic methodology have expanded the applications of L-Alanine, N-methyl-, ethyl ester, hydrochloride. A recent publication in Organic Letters (2024) described a novel, high-yield synthetic route that improves the scalability of production while maintaining excellent enantiomeric purity. This development addresses previous limitations in large-scale manufacturing, making the compound more accessible for both research and potential clinical applications.

Looking forward, the unique properties of L-Alanine, N-methyl-, ethyl ester, hydrochloride position it as a valuable tool in the development of next-generation therapeutics. Current research directions include its incorporation into mRNA delivery systems, where its amphiphilic character may enhance cellular uptake, and its use in the design of antimicrobial peptides with improved stability profiles. As synthetic biology and precision medicine continue to advance, this compound is likely to play an increasingly important role in bridging the gap between small molecule and biologic therapies.

In conclusion, recent studies on L-Alanine, N-methyl-, ethyl ester, hydrochloride (CAS: 117856-39-0) demonstrate its growing importance in pharmaceutical research and development. Its versatile applications in drug delivery, neurology, oncology, and synthetic chemistry highlight its potential to address multiple challenges in modern medicine. Continued research into its structure-activity relationships and optimization of its pharmacological properties will be crucial for translating these findings into clinical applications. The compound represents an excellent example of how chemical modifications of amino acids can yield molecules with significant therapeutic potential.

Recommended suppliers
Jiangsu Xinsu New Materials Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jiangsu Xinsu New Materials Co., Ltd
ASIACHEM I&E (JIANGSU) CO., LTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
ASIACHEM I&E (JIANGSU) CO., LTD
Inner Mongolia Xinhong Biological Technology Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Inner Mongolia Xinhong Biological Technology Co., Ltd
Zhejiang Brunova Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Zhejiang Brunova Technology Co., Ltd.
SunaTech Inc.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
SunaTech Inc.