| Name | Fmoc-D-Pipecolic Acid |
|---|---|
| Synonyms |
NALPHA-9-Fluorenylmethoxycbonyl-D-pipecolinic acid
MFCD00235899 (R)-N-FMOC-PIPERIDINE-2-CBOXYLIC ACID FMOC-D-HOPRO-OH (R)-1-Fmoc-2-piperidinecboxylic Acid Fmoc-D-Piperidine-2-cboxylic acid Fmoc-D-PIPE FMOC-(R)-PIPECOLINIC ACID N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-D-PIPECOLIC ACID (2R)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]hexahydropyridine-2-carboxylic acid FMOC-D-(+)-PIPECOLIC ACID 2-[9H-fluoren-9-ylmethoxy(oxo)methyl]-2-piperidinecboxylic acid (R)-PIPERIDINE-1,2-DICBOXYLIC ACID 1-(9H-FLUOREN-9-YLMETHYL) ESTER FMOC-D-HOMOPRO-OH FMOC-D-HOMOPROLINE (R)-N-Fmoc-piperidine-2-cboxyL (R)-PIPERIDINE-1 N-FMOC-D-PIPECOLINIC ACID (R)-N-(9-FLUORENYLMETHYLOXYCBONYL)-PIPERIDINE-2-CBOXYLIC ACID (D)-N-(9-FLUORENYLMETHYLOXYCBONYL)PIPECOLIC ACID N-alpha-(9-Fluorenyloxycbonyl)-piperidine-2S-cboxylicacid N-FMOC-(R)-PIPECOLINIC ACID FMOC-(R)-PIPERIDINE-2-CBOXYLIC ACID 1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-pipecolic Acid (R)-1-FMoc-piperidine-2-cboxylic acid (R)-N-Fmoc-piperidine-2-cboxylic acid, N-Fmoc-D-pipecolic acid (R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidine-2-carboxylic acid (D)-N-FMOC-PIPECOLIC ACID N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-D-HOMOPROLINE FMOC-D-PIP-OH (R)-Piperidine-2-cboxylic acid, N-FMOC protected D-1-FMOC-PIPECOLINIC ACID N-Fmoc-D-pipecolic acid (R)-N-FLUORENYLMETHOXYCBONYL-2-PIPERIDINECBOXYLIC ACID Fmoc-D-Homoproline 1-Fmoc-D-pipecolic Acid 1,2-Piperidinedicboxylicacid, 1-(9H-fluoren-9-ylMethyl) ester, (2R) (9H-Fluoren-9-yl)MethOxy]carbonyl D-HoPro-OH (R)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-cboxylic acid (R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecboxylic Acid FMOC-D-PIC(2)-OH (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid (2R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid RECHEM PA 0006 Fmoc-D-homoproline (HPLC) D-Pipecolinic acid, N-FMOC protected (2R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]piperidine-2-carboxylic acid 2-DICBOXYLIC ACID 1-(9H-FLUOREN-9-YLMETHYL) ESTER (2R)-1-[(9H-FLUOREN-9-YLMETHOXY)carbonyl]HEXAHYDROPYRIDINE-2-CBOXYLIC ACID (2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]piperidine-2-carboxylic acid (2R)-1-[(9H-FLUOREN-9-YLMETHOXY)carbonyl]PIPERIDINE-2-CBOXYLIC ACID Fmoc- D -Pip-OH Fmoc-D-HomoPro-OH N-FMoc-(R)-2-piperidinecboxylic acid N-ALPHA-FMOC-D-PIPECOLIC ACID FMOC-D-PIPECOLIC ACID FMOC-(R)-(+)-PIPERIDINE-2-CBOXYLIC ACID |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 561.6±43.0 °C at 760 mmHg |
| Melting Point | 149-153°C |
| Molecular Formula | C21H21NO4 |
| Molecular Weight | 351.396 |
| Flash Point | 293.5±28.2 °C |
| Exact Mass | 351.147064 |
| PSA | 66.84000 |
| LogP | 3.57 |
| Vapour Pressure | 0.0±1.6 mmHg at 25°C |
| Index of Refraction | 1.620 |
| Storage condition | 2-8°C |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xi |
| Risk Phrases | R36/37/38 |
| Safety Phrases | S26;S36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2933399090 |
|
~81%
101555-63-9 |
| Literature: Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V.; Gopalakrishnan, Ranganath; Hausch, Felix Patent: EP2607352 A1, 2013 ; Location in patent: Paragraph 0111 ; |
|
~82%
101555-63-9 |
| Literature: MAX-PLANCK-GESELLSCHAFT ZUR FÖRDERUNG DER WISSENSCHAFTEN E.V.; GOPALAKRISHNAN, Ranganath; HAUSCH, Felix Patent: WO2013/91900 A1, 2013 ; Location in patent: Page/Page column 41 ; |
|
~51%
101555-63-9 |
| Literature: Blizzard, Timothy A.; Singh, Sanjay; Patil, Basanagoud; Chidurala, Naresh; Komanduri, Venukrishnan; Debnath, Samarpita; Belyakov, Sergei; Crespo, Alejandro; Struck, Alice; Kurtz, Marc; Wiltsie, Judyann; Shen, Xun; Sonatore, Lisa; Arocho, Marta; Lewis, Dale; Ogletree, Martin; Biftu, Tesfaye Bioorganic and Medicinal Chemistry Letters, 2014 , vol. 24, # 4 p. 1111 - 1115 |
|
~84%
101555-63-9 |
| Literature: Gopalakrishnan, Ranganath; Kozany, Christian; Gaali, Steffen; Kress, Christoph; Hoogeland, Bastiaan; Bracher, Andreas; Hausch, Felix Journal of Medicinal Chemistry, 2012 , vol. 55, # 9 p. 4114 - 4122 |
|
~62%
101555-63-9 |
| Literature: Schoen, Istvan; Kisfaludy, Lajos Synthesis, 1986 , # 4 p. 303 - 305 |
|
~%
101555-63-9 |
| Literature: Journal of Organic Chemistry, , vol. 57, # 16 p. 4394 - 4400 |
|
~%
101555-63-9 |
| Literature: Journal of Organic Chemistry, , vol. 76, # 16 p. 6686 - 6693 |
| Precursor 7 | |
|---|---|
| DownStream 1 | |
| 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% |