Name | N-[(1,1-Dimethylethoxy)carbonyl]-O-(phenylmethyl)-L-serine |
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Synonyms |
BOC-SER-OTBU
Boc-L-Ser(OBzl)-OH N-(tert-butyloxycarbonyl)-O-benzyl-L-serine L-N-(t-butoxycarbonyl)-O-(benzyl)serine O-Benzyl-N-(tert-butoxycarbonyl)-L-serine BOC-SER(BU)-OH (S)-3-(Benzyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acid N-(tert-Butoxycarbonyl)-O-benzyl-L-serine Boc-D-Ser(Bzl)-OH N-tert-butoxycarbonyl-O-benzyl-L-serine Boc-Ser(Bzl)-OH BOC-SER(BUT)-OH BOC-Ser (Obzl) OH BOC-L-SER(TBU)-OH MFCD00079666 L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)- O-Benzyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-serine BOC-SERINE(TBU)-OH N-BOC-O-Benzyl-L-serine BOC-SER(TBU)-OH N-BOC-O-Benzyl-L-ser (2S)-3-(Benzyloxy)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)propanoic acid BOC-O-BENZYL-L-SER-OH EINECS 245-820-1 Boc-O-benzyl-L-serine |
Description | (S)-3-(Benzyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acid is a serine 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 | 456.2±45.0 °C at 760 mmHg |
Melting Point | 57-62ºC |
Molecular Formula | C15H21NO5 |
Molecular Weight | 295.331 |
Flash Point | 229.7±28.7 °C |
Exact Mass | 295.141968 |
PSA | 84.86000 |
LogP | 3.56 |
Vapour Pressure | 0.0±1.2 mmHg at 25°C |
Index of Refraction | 1.523 |
Storage condition | 2~8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xn |
Risk Phrases | R20/21/22 |
Safety Phrases | S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
~99% 23680-31-1 |
Literature: Gravestock, David; Rousseau, Amanda L.; Lourens, Anna C.U.; Hoppe, Heinrich C.; Nkabinde, Lindiwe A.; Bode, Moira L. Tetrahedron Letters, 2012 , vol. 53, # 26 p. 3225 - 3229 |
~96% 23680-31-1 |
Literature: Sajiki, Hironao; Hirota, Kosaku Tetrahedron, 1998 , vol. 54, # 46 p. 13981 - 13996 |
~93% 23680-31-1 |
Literature: Ramasamy, Kanda S.; Stoisavljevic, Vesna Nucleosides and Nucleotides, 1999 , vol. 18, # 8 p. 1845 - 1861 |
~71% 23680-31-1 |
Literature: Barcelo, Gerard; Senet, Jean-Pierre; Sennyey, Gerard; Bensoam, Jean; Loffet, Albert Synthesis, 1986 , # 8 p. 627 - 632 |
~% 23680-31-1 |
Literature: Journal of Medicinal Chemistry, , vol. 44, # 26 p. 4524 - 4534 |
~% 23680-31-1 |
Literature: Tetrahedron Letters, , vol. 53, # 26 p. 3225 - 3229 |
~% 23680-31-1 |
Literature: Chemical and pharmaceutical bulletin, , vol. 35, # 2 p. 468 - 478 |
~% 23680-31-1 |
Literature: Chemische Berichte, , vol. 97, p. 2497 - 2503 |
Precursor 8 | |
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DownStream 10 | |