Boc-L-glutamic acid 1-benzyl ester structure
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Common Name | Boc-L-glutamic acid 1-benzyl ester | ||
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CAS Number | 30924-93-7 | Molecular Weight | 337.368 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 522.6±50.0 °C at 760 mmHg | |
Molecular Formula | C17H23NO6 | Melting Point | 97 °C | |
MSDS | Chinese USA | Flash Point | 269.9±30.1 °C |
Use of Boc-L-glutamic acid 1-benzyl esterBoc-Glu-OBzl is a glutamic acid derivative[1]. |
Name | (4S)-4-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-5-phenylmethoxypentanoic acid |
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Synonym | More Synonyms |
Description | Boc-Glu-OBzl is a glutamic acid derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 522.6±50.0 °C at 760 mmHg |
Melting Point | 97 °C |
Molecular Formula | C17H23NO6 |
Molecular Weight | 337.368 |
Flash Point | 269.9±30.1 °C |
Exact Mass | 337.152527 |
PSA | 101.93000 |
LogP | 3.34 |
Vapour Pressure | 0.0±1.4 mmHg at 25°C |
Index of Refraction | 1.524 |
Storage condition | −20°C |
~80% Boc-L-glutamic ... CAS#:30924-93-7 |
Literature: Cantacuzene, D.; Pascal, F.; Guerreiro, C. Tetrahedron, 1987 , vol. 43, # 8 p. 1823 - 1826 |
~95% Boc-L-glutamic ... CAS#:30924-93-7 |
Literature: Sturtz; Appere; Breistol; Fodstad; Schwartsmann; Hendriks European Journal of Medicinal Chemistry, 1992 , vol. 27, # 8 p. 825 - 833 |
~% Boc-L-glutamic ... CAS#:30924-93-7 |
Literature: Chemical communications (Cambridge, England), , # 19 p. 1908 - 1909 |
~% Boc-L-glutamic ... CAS#:30924-93-7 |
Literature: Angewandte Chemie, , vol. 84, p. 259 |
~% Boc-L-glutamic ... CAS#:30924-93-7 |
Literature: Justus Liebigs Annalen der Chemie, , vol. 673, p. 196 - 207 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2924299090 |
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Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Stability and in vitro metabolism of dipeptide model prodrugs with affinity for the oligopeptide transporter.
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Side reactions in solid-phase peptide synthesis and their applications.
Int. J. Pept. Protein Res. 48 , 292-298, (1996) Side reactions in peptide synthesis indicate steps needing improvement as well as opportunities for structural diversification in combinatorial design. Among the side reactions observed in this study,... |
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Modification of the vitamin K-dependent carboxylase assay.
J. Biochem. Biophys. Methods 11 , 59, (1985) Methods are presented that describe alternative protocols for the isolation of rat liver microsomes containing the vitamin K-dependent carboxylase and the procedure in which the solubilized enzyme is ... |
N-α-tert-BOC-L-glutamic-γ-benzyl ester |
Boc-L-glutamic acid 1-benzyl ester |
(2S)-5-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) |
Boc-Glu-OBzl |
5-Benzyl N-(tert-Butoxycarbonyl)-L-glutamate |
L-Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 5-(phenylmethyl) ester |
Boc-L-glutamic acid 5-benzyl ester |
5-Benzyl N-Boc-L-glutamate |
MFCD00065568 |
N-t-butoxycarbonyl-L-glutamic acid benzyl ester |
B-Glu-BE |
Boc-(S)-glutamic acid benzyl ester |
(2S)-5-(Benzyloxy)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-oxopentanoic acid |
(4S)-5-(Benzyloxy)-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) |
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-5-phenylmethoxypentanoic acid |
Boc-L-Glutamicacid1-benzylester |
Boc-Glu(Obzl)-OH |
N-Boc-L-glutamic Acid 5-Benzyl Ester |
(4S)-5-(Benzyloxy)-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-oxopentanoic acid |
N-(tert-Butoxycarbonyl)-L-glutamic Acid 1-Benzyl Ester |
N-(tert-Butoxycarbonyl)-L-glutamic acid 5-benzyl ester |
Boc-L-Glutamic acid 5-benzylester |
Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl) ester |
N-Boc-L-glutamic Acid 1-Benzyl Ester |
1-Benzyl N-(tert-Butoxycarbonyl)-L-glutamate |
1-Benzyl N-Boc-L-glutamate |
Boc-L-glutamic acid α-benzylester |