Molecular structure of Acetyl-glycine methyl amide, CAS Number: 7606-79-3
Acetyl-glycine methyl amide (CAS 7606-79-3)
Alternate Names:
Ac-Gly-NHMe
Application:
Acetyl-glycine methyl amide is an acetamide compound for proteomics research
CAS Number:
7606-79-3
Molecular Weight:
130.15
Molecular Formula:
C5H10N2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Acetyl-glycine methyl amide is an acetamide compound for proteomics research. Acetyl-glycine methyl amide is an organic compound consisting of a nitrogen atom, two carbon atoms, and four hydrogen atoms. It is employed in scientific and laboratory research for various purposes. The compound demonstrates versatility and has been extensively examined for its potential biochemical and physiological impacts, as well as its efficacy in laboratory experiments. In scientific research, Acetyl-glycine methyl amide finds utility as a reagent for synthesizing other compounds like N-methylacetamide, and as a catalyst for the synthesis of substances such as N-methylpyrrole.
Acetyl-glycine methyl amide (CAS 7606-79-3) References
- Calorimetric studies of the interactions of guanidinium hydrochloride and potassium iodide with model amides in aqueous solution. | Stimson, ER. and Schrier, EE. 1975. Biopolymers. 14: 509-20. PMID: 1174678
- Role of water in structural changes of poly(AVGVP) and poly(GVGVP) Studied by FTIR and Raman spectroscopy and ab initio calculations. | Schmidt, P., et al. 2005. Biomacromolecules. 6: 697-706. PMID: 15762632
- Designing amino acid residues with single-conformations. | Tran, TT., et al. 2006. Protein Eng Des Sel. 19: 401-8. PMID: 16799150
- Use of constrained synthetic amino acids in beta-helix proteins for conformational control. | Zanuy, D., et al. 2007. J Phys Chem B. 111: 3236-42. PMID: 17388467
- A matrix isolation study on Ac-Gly-NHMe and Ac-l-Ala-NHMe, the simplest chiral and achiral building blocks of peptides and proteins. | Pohl, G., et al. 2007. Phys Chem Chem Phys. 9: 4698-708. PMID: 17700871
- Vibrational and chiroptical spectroscopic characterization of gamma-turn model cyclic tetrapeptides containing two beta-Ala residues. | Vass, E., et al. 2010. Chirality. 22: 762-71. PMID: 20155823
- β-turn tendency in N-methylated peptides with dehydrophenylalanine residue: DFT study. | Buczek, A., et al. 2012. Biopolymers. 97: 518-28. PMID: 22328238
- Electronic structure of hole-conducting states in polyprolines. | Monney, NP., et al. 2015. J Phys Chem B. 119: 6584-90. PMID: 25942020
- Understanding the conformational behaviour of Ac-Ala-NHMe in different media. A joint NMR and DFT study. | Cormanich, RA., et al. 2015. Org Biomol Chem. 13: 9206-13. PMID: 26219244
- Thermodynamic properties of aqueous osmolyte solutions at high-pressure conditions. | Knierbein, M., et al. 2019. Biophys Chem. 253: 106211. PMID: 31280070
- Theoretical analysis of conformations of Ac-Gly-L-Ala-Gly-NHMe with intramolecular hydrogen bonds. | Pletnev, VZ., et al. 1974. Biopolymers. 13: 1085-92. PMID: 4855178
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Acetyl-glycine methyl amide, 250 mg | sc-291803 | 250 mg | $54.00 | |||
Acetyl-glycine methyl amide, 1 g | sc-291803A | 1 g | $165.00 |