| Name | Fmoc-(S)-(-)-piperidine-2-carboxylic acid |
|---|---|
| Synonyms |
(S)-N-FLUORENYLMETHOXYCBONYL-2-PIPERIDINECBOXYLIC ACID
(S)-1,2-Piperidinedicboxylic acid 1-(9H-fluoren-9-ylmethyl) ester MFCD00235898 FMOC-L-PIPERIDINE-2-CBOXYLIC ACID (S)-Piperidine-2-cboxylic acid, N-FMOC protected L-1-N-FMOC-PIPECOLINIC ACID (S)-1-Fmoc-piperidine-2-cboxylic acid, N-Fmoc-L-pipecolinic acid (2S)-1-[9H-fluoren-9-ylmethoxy(oxo)methyl]-2-piperidinecboxylic acid FMOC-PIPERIDINE-2-CBOXYLIC ACID (S)-1-FMOC-PIPERIDINE-2-CBOXYLIC ACID (S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecboxylic Acid (9H-Fluoren-9-yl)MethOxy]carbonyl HoPro-OH FMOC-B-HOMO-PRO-OH N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-PIPECOLIC ACID FMOC-L-(-)-PIPECOLIC ACID N-FMoc-(S)-2-piperidinecboxylic acid 1-Fmoc-L-pipecolic Acid (S)-1-FMOC-PIPERIDINE-2-CARBOXYLIC ACID Fmoc-HoPro-OH N-FMOC-(S)-PIPECOLINIC ACID Fmo-L-homoproline (HPLC) 1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-pipecolic Acid FMOC-HOPRO-OH N-FMOC-L-PIPECOLINIC ACID S)-PIPERIDINE-1 2,2-Piperidinedicarboxylic acid, 2-(9H-fluoren-9-ylmethyl) ester (L)-N-FMOC-PIPECOLIC ACID (S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecboxylicAcid> 2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid FMOC-HOMOPROLINE N-Fmoc-(2S)-piperidinecboxylic acid (S)-N-(9-FLUORENYLMETHYLOXYCBONYL)-PIPERIDINE-2-CBOXYLIC ACID fmoc-l-pipecolic acid (S)-N-Fmoc-piperidine-2-cboxyL FMOC-L-PIP-OH (L)-N-(9-FLUORENYLMETHYLOXYCBONYL)PIPECOLIC ACID (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid FMO-L-HOMOPROLINE Fmoc-HomoPro-OH (S)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-cboxylic acid N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-HOMOPROLINE (S)-PIPERIDINE-1,2-DICBOXYLIC ACID 1-(9H-FLUOREN-9-YLMETHYL) ESTER Fmoc-Pip-OH,(S)-1-Fmoc-piperidine-2-cboxylic acid, N-Fmoc-L-pipecolinic acid (2S)-1-(9H-fluoren-9-ylmethoxycbonyl)piperidine-2-cboxylic acid L-Pipecolinic acid, N-FMOC protected (S)-N-Fmoc-piperidine-2-cboxylic acid RECHEM BK PT 0274 FMOC-(S)-(-)-PIPERIDINE-2-CBOXYLIC ACID N-ALPHA-FMOC-L-PIPECOLIC ACID Fmoc-β-Homo-Pro-OH (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]piperidine-2-carboxylic acid (S)-1-Fmoc-2-piperidinecboxylic Acid FMOC-PIC(2)-OH 1,2-Piperidinedicboxylicacid, 1-(9H-fluoren-9-ylMethyl) ester, (2S) (S)-1,2-Piperidinedicarboxylic acid 1-(9H-fluoren-9-ylmethyl) ester N-(9-Fluorenyloxycbonyl)-piperidine-2R-cboxylicacid FMOC-PIP-OH FMOC-L-HOMOPROLINE Fmoc-L-PIPE FMOC-L-PIPECOLIC ACID //BP FMOC-HOMOPRO-OH N-FMoc-L-pipecolic acid FMOC-L-PIPECOLIC ACID |
| Description | Fmoc-HoPro-OH is a proline 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 | 1.293±0.06 g/cm3 |
|---|---|
| Boiling Point | 553.7±50.0 °C at 760 mmHg |
| Melting Point | 161-162.5 ºC |
| Molecular Formula | C21H21NO4 |
| Molecular Weight | 351.396 |
| Flash Point | 288.7±30.1 °C |
| Exact Mass | 351.147064 |
| PSA | 66.84000 |
| LogP | 3.92 |
| Vapour Pressure | 0.0±1.6 mmHg at 25°C |
| Index of Refraction | 1.608 |
| Storage condition | 2-8°C |
| Water Solubility | Insuluble (8.8E-3 g/L) (25 ºC) |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi: Irritant; |
| RIDADR | UN 3077 9 / PGIII |
| WGK Germany | 3 |
| HS Code | 2933399090 |
| HS Code | 2933399090 |
|---|---|
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |