Products Categories
CAS No.: | 13574-13-5 |
---|---|
Name: | Boc-L-Glutamic acid 5-benzylester |
Article Data: | 31 |
Molecular Structure: | |
Formula: | C17H23NO6 |
Molecular Weight: | 337.373 |
Synonyms: | 5-Benzyl N-((1,1-dimethylethoxy)carbonyl)-L-glutamate;L-Glutamic acid, N-((1,1-dimethylethoxy)carbonyl)-, 5-(phenylmethyl) ester;Boc-Glu(OBzl)-OH;Boc-L-glutamic acid 5 benzyl ester;Boc-L-glutamic acid γ-benzyl ester; |
EINECS: | 237-007-5 |
Density: | 1.197 g/cm3 |
Melting Point: | 69-71 °C |
Boiling Point: | 522.6 °C at 760 mmHg |
Flash Point: | 269.9 °C |
Appearance: | white to off-white powder |
Safety: | 22-24/25 |
PSA: | 101.93000 |
LogP: | 2.87880 |
What can I do for you?
Get Best Price
The Boc-L-Glutamic acid 5-benzylester, with the CAS registry number 13574-13-5 and EINECS registry number 237-007-5, has the systematic name of (2S)-5-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name). It belongs to the following product categories: Amino Acids; Glutamic acid [Glu, E]; Boc-Amino Acids and Derivative; Amino Acids (N-Protected); Biochemistry; Boc-Amino Acids; Boc-Amino acid series. And molecular formula of the chemical is C17H23NO6. What's more, while dealing with this chemical, you should not breathe dust and then try to avoid contacting with skin and eyes.
The characteristics of Boc-L-Glutamic acid 5-benzylester are as followings: (1)ACD/LogP: 3.34; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.21; (4)ACD/LogD (pH 7.4): -0.23; (5)ACD/BCF (pH 5.5): 1.51; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 11.58; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 7; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 10; (12)Polar Surface Area: 82.14 Å2; (13)Index of Refraction: 1.523; (14)Molar Refractivity: 86.13 cm3; (15)Molar Volume: 281.6 cm3; (16)Polarizability: 34.14×10-24cm3; (17)Surface Tension: 46 dyne/cm; (18)Density: 1.197 g/cm3; (19)Flash Point: 269.9 °C; (20)Enthalpy of Vaporization: 83.81 kJ/mol; (21)Boiling Point: 522.6 °C at 760 mmHg; (22)Vapour Pressure: 9.49E-12 mmHg at 25°C.
Synthesis methods of Boc-L-Glutamic acid 5-benzylester: It can be produce by benzoic alcohol and tert-Butoxycarbonyl-L-glutamic acid. It is a kind of esterification reaction, and then it also need purification by Crystallization.
Addtionally, the following datas could be converted into the molecular structure:
(1)SMILES: O=C(OC(C)(C)C)N[C@H](C(=O)O)CCC(=O)OCc1ccccc1
(2)InChI: InChI=1/C17H23NO6/c1-17(2,3)24-16(22)18-13(15(20)21)9-10-14(19)23-11-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,18,22)(H,20,21)/t13-/m0/s1
(3)InChIKey: AJDUMMXHVCMISJ-ZDUSSCGKBU