Cas no 90495-99-1 (2-2-(Boc-amino)ethylaminoacetic Acid)

2-2-(Boc-amino)ethylaminoacetic Acid is a protected amino acid derivative featuring a Boc (tert-butoxycarbonyl) group, which serves as a key intermediate in peptide synthesis and organic chemistry applications. The Boc group provides stability under basic conditions while allowing selective deprotection under acidic conditions, making it valuable for stepwise peptide elongation. Its ethylaminoacetic acid backbone offers versatility in modifying molecular structures, particularly in drug discovery and bioconjugation. The compound is characterized by high purity and consistent reactivity, ensuring reliable performance in complex synthetic pathways. Its compatibility with standard coupling reagents further enhances its utility in solid-phase and solution-phase peptide synthesis.
2-2-(Boc-amino)ethylaminoacetic Acid structure
90495-99-1 structure
Product Name:2-2-(Boc-amino)ethylaminoacetic Acid
CAS No:90495-99-1
MF:C9H18N2O4
MW:218.250222682953
MDL:MFCD11974252
CID:788671
PubChem ID:9834393
Update Time:2025-05-26

2-2-(Boc-amino)ethylaminoacetic Acid Chemical and Physical Properties

Names and Identifiers

    • Glycine, N-[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]-
    • 2-[[2-(Boc-amino)ethyl]amino]acetic Acid
    • 2-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethylamino]acetic acid
    • ({2-[(tert-butoxycarbonyl)amino]ethyl}amino)acetic acid
    • (N'-Boc-2'-Aminoethyl)glycine N-(2-Boc-Aminoethyl)glycine
    • 2-[(2-(tert-butoxycarbonyl)amino)ethylamino]acetic acid
    • Glycine,N-[2-[[(1,1-dimethylethoxy)carbonyl]amino]ethyl]
    • N-(2-Boc-aminoethyl)glycine
    • N-(2-N-Boc-aminoethyl)glycine
    • N-[2-(tert-Butyloxycarbonylamino)ethyl]glycine
    • N-[2-[[(1,1-Dimethylethoxy)carbonyl]amino]ethyl]glycine
    • (N'-Boc-2'-aminoethyl)glycine
    • H-(Boc-NHEtGly)-OH
    • (N-Boc-2-aminoethyl)glycine
    • [2-(Boc-Amino)ethyl]-Gly-OH
    • LZQSLXNZORCPAR-UHFFFAOYSA-N
    • (N'-Boc-2'-aminoethyl) glycine
    • SY033323
    • 2-[[2-(Boc-amino)ethyl]amino]aceticAcid
    • M
    • CS-0372602
    • SCHEMBL2153073
    • N-alpha-(2-t-Butoxycarbonyl-aminoethyl)-glycine
    • AC1035
    • FT-0770110
    • CS-11924
    • MFCD11974252
    • AKOS027256645
    • A860789
    • DTXSID00431471
    • N-(2-tert-butoxycarbonylaminoethyl)aminoacetic acid
    • 90495-99-1
    • EN300-135497
    • 2-[(2-{[(tert-butoxy)carbonyl]amino}ethyl)amino]acetic acid
    • 2-((2-((tert-Butoxycarbonyl)amino)ethyl)amino)acetic acid
    • DA-40689
    • 2-[N-[2-(BOC-AMINO)ETHYL]AMINO]ACETIC ACID
    • 2-2-(Boc-amino)ethylaminoacetic Acid
    • MDL： MFCD11974252
    • Inchi： 1S/C9H18N2O4/c1-9(2,3)15-8(14)11-5-4-10-6-7(12)13/h10H,4-6H2,1-3H3,(H,11,14)(H,12,13)
    • InChI Key： LZQSLXNZORCPAR-UHFFFAOYSA-N
    • SMILES： O(C(NCCNCC(=O)O)=O)C(C)(C)C

Computed Properties

  • Exact Mass: 218.12700
  • Monoisotopic Mass: 218.12665706g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 7
  • Complexity: 223
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 87.7
  • XLogP3: -2.2

Experimental Properties

  • Color/Form: No data avaiable
  • Density: 1.131±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: No data available
  • Boiling Point: 380.2±27.0 °C at 760 mmHg
  • Flash Point: 183.8±23.7 °C
  • Solubility: Slightly soluble (18 g/l) (25 o C),
  • PSA: 91.15000
  • LogP: 0.78060
  • Vapor Pressure: No data available

2-2-(Boc-amino)ethylaminoacetic Acid Security Information

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abcr
AB526796-250 mg
2-[[2-(Boc-Amino)ethyl]amino]acetic acid, 95%; .
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2-2-(Boc-amino)ethylaminoacetic Acid Production Method

2-2-(Boc-amino)ethylaminoacetic Acid Suppliers

Amadis Chemical Company Limited
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(CAS:90495-99-1)2-2-(Boc-amino)ethylaminoacetic Acid
Order Number:A860789
Stock Status:in Stock
Quantity:1g/5g/10g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 08:26
Price ($):366.0/1080.0/1836.0

2-2-(Boc-amino)ethylaminoacetic Acid Related Literature

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Additional information on 2-2-(Boc-amino)ethylaminoacetic Acid

2-2-(Boc-amino)ethylaminoacetic Acid (CAS No. 90495-99-1): A Comprehensive Overview

The compound 2-2-(Boc-amino)ethylaminoacetic Acid, identified by the CAS number 90495-99-1, is a significant molecule in the field of organic chemistry and biochemistry. This compound is characterized by its unique structure, which includes a Boc (tert-butoxycarbonyl) protecting group attached to an aminoethyl group, further connected to a glycine moiety. The presence of the Boc group makes this compound particularly useful in peptide synthesis and other applications where controlled deprotection is required.

Recent advancements in chemical synthesis have highlighted the versatility of 2-2-(Boc-amino)ethylaminoacetic Acid. Researchers have explored its role in the construction of complex peptide libraries, where its Boc group serves as a reliable protective unit during multi-step synthesis. The ability to selectively remove the Boc group under mild acidic conditions has made this compound a valuable tool in medicinal chemistry, enabling the precise control of amino group availability during drug design processes.

In addition to its synthetic applications, 2-2-(Boc-amino)ethylaminoacetic Acid has shown promise in biological studies. Its structure allows for interactions with various biomolecules, making it a potential candidate for investigating enzyme-substrate interactions or as a component in bioconjugate chemistry. Recent studies have demonstrated its utility in the development of bioactive molecules, particularly in the context of targeted drug delivery systems.

The CAS number 90495-99-1 uniquely identifies this compound within chemical databases, ensuring accurate referencing and retrieval of related information. This is crucial for researchers who rely on standardized identifiers to access up-to-date literature and data on chemical properties, safety profiles, and applications.

In terms of physical properties, 2-2-(Boc-amino)ethylaminoacetic Acid exhibits a melting point that aligns with typical Boc-containing amino acids, reflecting its stability under various conditions. Its solubility characteristics make it suitable for use in both aqueous and organic solvents, depending on the specific application requirements.

The latest research trends indicate a growing interest in leveraging 2-2-(Boc-amino)ethylaminoacetic Acid's properties for advanced materials science applications. For instance, its ability to form self-assembled monolayers has been explored for use in nanotechnology and surface modification techniques. These findings underscore the compound's potential beyond traditional chemical synthesis, opening new avenues for interdisciplinary research.

In conclusion, 2-2-(Boc-amino)ethylaminoacetic Acid (CAS No. 90495-99-1) stands as a versatile and valuable molecule in modern chemistry. Its unique structure, combined with the functionality provided by the Boc group, positions it as an essential component in various scientific and industrial applications. As research continues to uncover new uses for this compound, its significance within the chemical community is likely to grow further.

90495-99-1 (2-2-(Boc-amino)ethylaminoacetic Acid) Related Products

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Amadis Chemical Company Limited
(CAS:90495-99-1)2-2-(Boc-amino)ethylaminoacetic Acid
A860789
Purity:99%/99%/99%
Quantity:1g/5g/10g
Price ($):366.0/1080.0/1836.0
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