| Name | (2S,4R)-4-fluoro-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid |
|---|---|
| Synonyms |
(2R,4S)-N-BOC-4-FLUORO-D-PROLINE
(2S,4R)-4-fluoro-1-[(2-methylpropan-2-yl)oxycbonyl]pyrrolidine-2-cboxylicaci Boc-trans-4F-Pro trans-1-(tert-Butoxycbonyl)-4-fluoropyrrolidine-2-cboxylicacid Boc-trans-4-Fluoro-L-proline (2S,4R)-4-Fluoropyrrolidine-2-cboxylic acid, N4-BOC protected N-T-BOC-TRANS-4-FLUORO-L-PROLINE (4R)-1-(tert-Butoxycarbonyl)-4-fluor-L-prolin (2S,4R)-4-FLUORO-PYRROLIDINE-1,2-DICBOXYLIC ACID 1-TERT-BUTYL ESTER 1-(1,1-Dimethylethyl) (2S,4R)-4-fluoro-1,2-pyrrolidinedicboxylate 1-(tert-butoxycarbonyl)-(4R)-fluoropyrrolidine-(2S)-carboxylic acid (2S,4R)-1-Boc-4-fluoropyrrolidine-2-cboxylic acid (2S,4R)-1-Boc-4-fluoro-2-pyrrolidinecboxylic Acid (4R)-4-Fluoro-1-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-proline N-Boc-Tran-4-Fluoro-L-proline BOC-TRANS-4-FLUORO-L-PROLINE //BP (2S,4R)-4-fluoro-1-[(2-methylpropan-2-yl)oxycbonyl]pyrrolidine-2-cboxylic acid (2S,4R)-1-(tert-Butoxycbonyl)-4-fluoro-2-pyrrolidinecboxylic Acid > (2S,4R)-1-(tert-Butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid N-(tert-Butoxycarbonyl)-(2S,4R)-4-fluoroproline N-BOC-TRANS-4-FLUORO-L-PROLINE (2S,4R)-Boc-4-fluoro-pyrrolidine-2-cboxylic acid N-(TERT-BUTOXYCBONYL)-(2S,4R)-4-FLUOROPROLINE N-Boc-trans-4-fluoro-L-proline (2S,4R)-1-(tert-Dutoxycbonyl)-4-fluoropyrrolidine-2-cboxylic acid N-BOC-(4S,2R)-4-FLUORO-2-PYRROLIDINECBOXYLIC ACID N-(tert-Butoxycbonyl)-trans-4-fluoro-L-proline (2S,4R)-4-Fluoropyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 1-BOC-Trans-4-fluoro-L-proline N-BOC-(2S,4R)-4-fluoro-2-pyrrolidinecboxylic acid N-Boc-trans-4-fluoro- L -proline (2R,4S)-N-Boc-trans-4-Fluoro-D-proline (2S,4R)-1-Boc-4-fluoro-2-pyrrolidinecarboxylic Acid Boc-trans-4-fluoro-Pro-OH (2S,4R)-1-(tert-butoxycbonyl)-4-fluoropyrrolidine-2-cboyxlic acid (4R)-1-(tert-Butoxycarbonyl)-4-fluoro-L-proline (2S,4R)-N-Boc-trans-4-Fluoro-L-Proline (2S,4R)-1-(tert-Butoxycbonyl)-4-fluoro-2-pyrrolidinecboxylic Acid N-(tert-Butoxycarbonyl)-trans-4-fluoro-L-proline 1,2-Pyrrolidinedicboxylic acid, 4-fluoro-, 1-(1,1-dimethylethyl) ester, (2S,4R) (2S,4R)-4-Fluoropyrrolidine-2-cboxylic acid, N-BOC protected (2S,4R)-1-(tert-Butoxycarbonyl)-4-fluoro-2-pyrrolidinecarboxylic Acid (2S,4R)-1-Boc-4-fluoro-2-pyrrolidinecboxylic Acid N-(tert-Butoxycbonyl)-trans-4-fluoro-L-proline N-Boc-trans-4-fluoro-L-proline MFCD06796085 BOC-TRANS-4-FLUORO-L-PROLINE trans-4-Fluoro-L-proline, N-BOC protected Boc-trans-4-F-Pro-OH (2R,4S)-N-Boc-trans-4-Fluoro-D-proline methyl ester TIANFU CHEM -BOC-TRANS-4-FLUORO-L-PROLINE (2S,4R)-4-Fluoro-1,2-pyrrolidinedicboxylic Acid tert-B utyl Ester (2S,4R)-4-fluoro-1,2-pyrrolidinedicarboxylic acid 1,1-dimethylethylester (2S,4R)-N-Boc-4-fluoroproline (2S,4R)-N-Boc-4-fluoropyrrolidine-2-cboxy lic acid trans-4-Fluoro-L-proline,N-BOC protected 1-(tert-Butyl) (2S,4R)-4-fluoro-1,2-pyrrolidinedicboxylate |
| Description | N-Boc-trans-4-fluoro-L-proline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
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| Related Catalog |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 346.0±42.0 °C at 760 mmHg |
| Melting Point | 115-119ºC |
| Molecular Formula | C10H16FNO4 |
| Molecular Weight | 233.24 |
| Flash Point | 163.0±27.9 °C |
| Exact Mass | 233.106339 |
| PSA | 66.84000 |
| LogP | 0.48 |
| Vapour Pressure | 0.0±1.6 mmHg at 25°C |
| Index of Refraction | 1.488 |
| 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-S36/37 |
| RIDADR | NONH for all modes of transport |
| HS Code | 2933990090 |
|
~99%
203866-14-2 |
| Literature: Hodges, Jonathan A.; Raines, Ronald T. Journal of the American Chemical Society, 2005 , vol. 127, # 45 p. 15923 - 15932 |
|
~99%
203866-14-2 |
| Literature: Chiba, Jun; Takayama, Gensuke; Takashi, Tohru; Yokoyama, Mika; Nakayama, Atsushi; Baldwin, John J.; McDonald, Edward; Moriarty, Kevin J.; Sarko, Christopher R.; Saionz, Kurt W.; Swanson, Robert; Hussain, Zahid; Wong, Angela; MacHinaga, Nobuo Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 8 p. 2725 - 2746 |
|
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203866-14-2 |
| Literature: Journal of the American Chemical Society, , vol. 127, # 45 p. 15923 - 15932 |
|
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203866-14-2 |
| Literature: Journal of the American Chemical Society, , vol. 127, # 45 p. 15923 - 15932 |
|
~%
203866-14-2 |
| Literature: Journal of the American Chemical Society, , vol. 125, # 31 p. 9262 - 9263 |
|
~%
203866-14-2 |
| Literature: Bioorganic and Medicinal Chemistry, , vol. 14, # 8 p. 2725 - 2746 |
|
~%
203866-14-2 |
| Literature: Tetrahedron Letters, , vol. 39, # 10 p. 1169 - 1172 |
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~%
203866-14-2 |
| Literature: Tetrahedron Letters, , vol. 39, # 10 p. 1169 - 1172 |
| Precursor 8 | |
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| DownStream 2 | |
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |