The Glycine, leucyl- (9CI), with the CAS registry number 615-82-7, is also known as DL-Leucylglycine and 2-(2-Amino-4-methylpentanoylamino)acetic acid. It belongs to the product categories of Amino Acid Derivatives; Biochemistry; Oligopeptides; Peptide Synthesis. Its EINECS registry number is 210-449-6. This chemical's molecular formula is C₈H₁₆N₂O₃ and molecular weight is 188.22. What's more, its systematic name is called Leucylglycine.

Physical properties about this chemical are: (1)ACD/LogP: -0.09; (2)#of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -2.59; (4)ACD/LogD (pH 7.4): -2.68; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 5; (10)#H bond donors: 4; (11)#Freely Rotating Bonds: 6; (12)Polar Surface Area: 49.85 Å²; (13)Index of Refraction: 1.488; (14)Molar Refractivity: 47.75 cm³; (15)Molar Volume: 165.5 cm³; (16)Surface Tension: 45 dyne/cm; (17)Density: 1.136 g/cm³; (18)Flash Point: 202 °C; (19)Enthalpy of Vaporization: 72.71 kJ/mol; (20)Boiling Point: 410.4 °C at 760 mmHg; (21)Vapour Pressure: 6.97E-08 mmHg at 25 °C.

Uses of Glycine, leucyl- (9CI): it is used to produce other chemicals. For example, it is used to produce 2-Amino-4,6-di-tert-butyl-phenol and N-(4-Methyl-2-oxo-valeryl)-glycine.

The reaction occurs with solvents Ethanol, H₂O and other condition of heating for 5 hours. The yield is 20%.

You can still convert the following datas into molecular structure:
(1) SMILES: O=C(NCC(=O)O)C(N)CC(C)C
(2) InChI: InChI=1/C8H16N2O3/c1-5(2)3-6(9)8(13)10-4-7(11)12/h5-6H,3-4,9H2,1-2H3,(H,10,13)(H,11,12)
(3) InChIKey: LESXFEZIFXFIQR-UHFFFAOYAD