Name | boc-val-gly-oh |
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Synonyms |
BOC-Val-Gly
Boc-L-valine methyl ester N-t-butoxycarbonyl-L-valine methyl ester BOC VALINE METHYLESTER Boc-L-Val-OMe Boc-Val-OMe N-Boc-L-Val-OMe N-Boc-L-valine methyl ester N-t-butoxycarbonyl-L-valylglycine |
Description | (tert-Butoxycarbonyl)-L-valylglycine is a Glycine (HY-Y0966) 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 |
Molecular Formula | C12H22N2O5 |
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Molecular Weight | 274.31300 |
Exact Mass | 274.15300 |
PSA | 104.73000 |
LogP | 1.51830 |
Index of Refraction | 1.479 |
RIDADR | NONH for all modes of transport |
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HS Code | 2924199090 |
~96% 45233-75-8 |
Literature: Chen, Yulin; Guan, Zhibin Journal of the American Chemical Society, 2010 , vol. 132, # 13 p. 4577 - 4579 |
~99% 45233-75-8 |
Literature: Bossler, Hans G.; Seebach, Dieter Helvetica Chimica Acta, 1994 , vol. 77, # 4 p. 1124 - 1165 |
~% 45233-75-8 |
Literature: Linge Gowda; Kumara; Channe Gowda; Rangappa International Journal of Chemical Kinetics, 2006 , vol. 38, # 6 p. 376 - 385 |
~96% 45233-75-8 |
Literature: Dutta, Anand S.; Giles, Michael B.; Williams, Joseph C. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1986 , p. 1655 - 1664 |
~% 45233-75-8 |
Literature: Skiles; Fuchs; Miao; Sorcek; Grozinger; Mauldin; Vitous; Mui; Jacober; Chow; Matteo; Skoog; Weldon; Possanza; Keirns; Letts; Rosenthal Journal of Medicinal Chemistry, 1992 , vol. 35, # 4 p. 641 - 662 |
Precursor 5 | |
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DownStream 0 |
HS Code | 2924199090 |
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Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |