DL-Alanine, N-carboxy-, N-benzyl ester(6CI,7CI) N-Carbobenzoxy-DL-alanine Z-DL-Ala-OH
The CAS register number of Alanine,N-[(phenylmethoxy)carbonyl]- is 4132-86-9. It also can be called as N-Benzyloxycarbonyl-DL-alanine and the IUPAC name about this chemical is 2-(phenylmethoxycarbonylamino)propanoic acid. The molecular formula about this chemical is C11H13NO4 and the molecular weight is 223.23. It belongs to the following product categories which include Amino Acids and Derivatives; Amino Acids; Amino Acids (N-Protected); Biochemistry; Cbz-Amino Acids and so on. When you are using it, please avoid contact with skin and eyes.
Physical properties about Alanine,N-[(phenylmethoxy)carbonyl]- are: (1)ACD/LogP: 1.71; (2)ACD/LogD (pH 5.5): -0.25; (3)ACD/LogD (pH 7.4): -1.79; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 2.23; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 5; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 5; (11)Polar Surface Area: 55.84Å2; (12)Index of Refraction: 1.544; (13)Molar Refractivity: 56.59 cm3; (14)Molar Volume: 179 cm3; (15)Polarizability: 22.43x10-24cm3; (16)Surface Tension: 49.5 dyne/cm; (17)Flash Point: 209.1 °C; (18)Enthalpy of Vaporization: 71.29 kJ/mol; (19)Boiling Point: 422.1 °C at 760 mmHg; (20)Vapour Pressure: 7.05E-08 mmHg at 25°C.
Preparation: this chemical can be prepared by carbonochloridic acid benzyl ester and L-alanine. The yield is about 70%.
Uses of Alanine,N-[(phenylmethoxy)carbonyl]-: it can be used to produce Carbobenzoxy-alaninanilid with aniline at temperature of 0 - 20 ℃. This reaction will need reagent CDMT, NMM and solvent tetrahydrofuran. The yield is about 93%.
The CAS register number of Alanine,N-[(phenylmethoxy)carbonyl]- is 4132-86-9. It also can be called as N-Benzyloxycarbonyl-DL-alanine and the IUPAC name about this chemical is 2-(phenylmethoxycarbonylamino)propanoic acid. The molecular formula about this chemical is C11H13NO4 and the molecular weight is 223.23. It belongs to the following product categories which include Amino Acids and Derivatives; Amino Acids; Amino Acids (N-Protected); Biochemistry; Cbz-Amino Acids and so on. When you are using it, please avoid contact with skin and eyes.
Physical properties about Alanine,N-[(phenylmethoxy)carbonyl]- are: (1)ACD/LogP: 1.71; (2)ACD/LogD (pH 5.5): -0.25; (3)ACD/LogD (pH 7.4): -1.79; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 2.23; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 5; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 5; (11)Polar Surface Area: 55.84Å2; (12)Index of Refraction: 1.544; (13)Molar Refractivity: 56.59 cm3; (14)Molar Volume: 179 cm3; (15)Polarizability: 22.43x10-24cm3; (16)Surface Tension: 49.5 dyne/cm; (17)Flash Point: 209.1 °C; (18)Enthalpy of Vaporization: 71.29 kJ/mol; (19)Boiling Point: 422.1 °C at 760 mmHg; (20)Vapour Pressure: 7.05E-08 mmHg at 25°C.
Preparation: this chemical can be prepared by carbonochloridic acid benzyl ester and L-alanine. The yield is about 70%.
Uses of Alanine,N-[(phenylmethoxy)carbonyl]-: it can be used to produce Carbobenzoxy-alaninanilid with aniline at temperature of 0 - 20 ℃. This reaction will need reagent CDMT, NMM and solvent tetrahydrofuran. The yield is about 93%.
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