| Name | Boc-alpha-Cyclohexyl-D-glycine |
|---|---|
| Synonyms |
BOC-D-2-CYCLOHEXYLGLYCINE
(2R)-2-[(tert-Butoxycbonyl)amino]-2-(cyclohexyl)ethanoic Acid N-Boc-D-cyclohexylglycine (R)-2-(Boc-amino)-2-cyclohexylacetic Acid BOC-D-CHG-OH H2O BOC-CYCLOHEXYL-D-GLYCINE N-tert-Butoxycbonyl-D-ALPHA-cyclohexylglycine Boc-(R)-2-Cyclohexylglycine (alph-alpha-[N-BOC-Amino]cyclohexaneacetic acid BOC-D-PHG(HEXAHYDRO)-OH H2O Boc-D-Cyclohexyglycine BOC-D-CHG-OH N-(tert-butoxycbonyl) cyclohexyl glycine BOC-D-CGL-OH (2R)-Cyclohexyl({[(2-methyl-2-propanyl)oxy]carbonyl}amino)acetic acid N-ALPHA-BUTOXYCBONYL-HEXAHYDRO-D-PHENYLGLYCINE HYDRATE N-tert-Butoxycbonyl-D-cyclohexyl (Tert-Butoxy)carbonyl D-Chg-OH N-(tert-Butoxycbonyl)-D-2-cyclohexylglycine > (R)-2-(tert-butoxycbonylamino)-2-cyclohexylacetic acid BOC-CYCLOHEXYL-D-GLY-OH Boc-D-2-cyclohexylglycine (TLC) (2R)-2-cyclohexyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid N-BOC-2-CYCLOHEXYL-D-GLYCINE MFCD05662178 Boc-D-Cyclohexylglycine (Boc-D-Cgl-OH) R-Boc-D-Cyclohexylglycine Boc-D-Chg-OH BOC-D-CYCLOHEXYLGLYCINE Boc-alpha-Cyclohexyl-D-glycine //BP (2R)-2-cyclohexyl-2-[(2-methylpropan-2-yl)oxycbonylamino]acetic acid 2-[[2-[(2-methylpropan-2-yl)oxy-oxomethyl]cyclohexyl]amino]acetic acid N-Boc-D-cycL (2R)-[(tert-Butoxycarbonyl)amino](cyclohexyl)acetic acid N-ALPHA-BUTOXYCBONYL-D-CYCLOHEXYLGLYCINE BOC-D-CLGL-OH H2O BOC-D-ALPHA-CYCLOHEXYLGLYCINE (2R)-2-{[(tert-butoxy)carbonyl]amino}-2-cyclohexylacetic acid (αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclohexaneacetic acid N-(tert-Butoxycbonyl)-D-2-cyclohexylglycine Cyclohexaneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αR) (R)-N-Boc-amino-cyclohexyl-acetic acid N-Boc-D-2-cyclohexylglycine (R)-TERT-BUTOXYCBONYLAMINO-CYCLOHEXYL-ACETIC ACID N-ALPHA-BUTOXYCBONYL-D-CYCLOHEXYLGLYCINE HYDRATE Boc-D-α-cyclohexylglycine |
| Description | Boc-D-Chg-OH is a Glycine (HY-Y0966) derivative[1]. |
|---|---|
| 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 | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 407.9±28.0 °C at 760 mmHg |
| Melting Point | 75 °C |
| Molecular Formula | C13H23NO4 |
| Molecular Weight | 257.326 |
| Flash Point | 200.5±24.0 °C |
| Exact Mass | 257.162720 |
| PSA | 75.63000 |
| LogP | 3.16 |
| Vapour Pressure | 0.0±2.0 mmHg at 25°C |
| Index of Refraction | 1.490 |
| Storage condition | 2-8°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xn |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
|
~89%
70491-05-3 |
| Literature: King, Amber M.; Salome, Christophe; Dinsmore, Jason; Salome-Grosjean, Elise; De Ryck, Marc; Kaminski, Rafal; Valade, Anne; Kohn, Harold Journal of Medicinal Chemistry, 2011 , vol. 54, # 13 p. 4815 - 4830 |
|
~%
70491-05-3 |
| Literature: Advanced Synthesis and Catalysis, , vol. 346, # 9-10 p. 1131 - 1140 |
|
~%
70491-05-3 |
| Literature: Advanced Synthesis and Catalysis, , vol. 346, # 9-10 p. 1131 - 1140 |
|
~%
70491-05-3 |
| Literature: Advanced Synthesis and Catalysis, , vol. 346, # 9-10 p. 1131 - 1140 |
|
~%
70491-05-3 |
| Literature: Advanced Synthesis and Catalysis, , vol. 346, # 9-10 p. 1131 - 1140 |
|
~%
70491-05-3 |
| Literature: Tetrahedron, , vol. 53, # 4 p. 1275 - 1294 |
|
~78%
70491-05-3 |
| Literature: Notz, Wolfgang; Watanabe, Shin-Ichi; Chowdari, Naidu S.; Zhong, Guofu; Betancort, Juan M.; Tanaka, Fujie; Barbas III, Carlos F. Advanced Synthesis and Catalysis, 2004 , vol. 346, # 9-10 p. 1131 - 1140 |
| Precursor 6 | |
|---|---|
| DownStream 2 | |