5680-79-5 | Glycine methyl ester hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$8.00	$5.00
5g	97%	in stock	$9.00	$6.00
10g	97%	in stock	$10.00	$7.00
25g	97%	in stock	$20.00	$14.00
100g	97%	in stock	$20.00	$14.00
500g	97%	in stock	$26.00	$18.00

Description

• Catalog Number: AB46214
• Chemical Name: Glycine methyl ester hydrochloride
• CAS Number: 5680-79-5
• Molecular Formula: C3H8ClNO2
• Molecular Weight: 125.5541
• MDL Number: MFCD00012870
• SMILES: COC(=O)CN.Cl
• NSC Number: 9229

Computed Properties

• Complexity: 52.8
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Literature

• Glycine enolates: the effect of formation of iminium ions to simple ketones on alpha-amino carbon acidity and a comparison with pyridoxal iminium ions.

  Journal of the American Chemical Society 20080213

• New zinc(II)-based catalyst for asymmetric azomethine ylide cycloaddition reactions.

  Organic letters 20061012

• Positive charges on lysine residues of the extrinsic 18 kDa protein are important to its electrostatic interaction with spinach photosystem II membranes.

  Acta biochimica et biophysica Sinica 20051101

• Cu(I)-catalyzed highly exo-selective and enantioselective [3 + 2] cycloaddition of azomethine ylides with acrylates.

  Organic letters 20050915

• Efficient microwave combinatorial parallel and nonparallel synthesis of N-alkylated glycine methyl esters as peptide building blocks.

  Journal of combinatorial chemistry 20050101

• Identification of domains on the extrinsic 23 kDa protein possibly involved in electrostatic interaction with the extrinsic 33 kDa protein in spinach photosystem II.

  European journal of biochemistry 20040301

• Sweetness and enzymatic activity of lysozyme.

  Journal of agricultural and food chemistry 20011001

• Effect of modification of the carboxyl groups of the sialic acid binding lectin from bullfrog (Rana catesbeiana) oocyte on anti-tumor activity.

  Biological & pharmaceutical bulletin 20010901

• Glycine enolates: the large effect of iminium ion formation on alpha-amino carbon acidity.

  Journal of the American Chemical Society 20010815