| Identification | More | [Name]
FMOC-D-Valine | [CAS]
84624-17-9 | [Synonyms]
9-FLUORENYLMETHOXYCARBONYL-D-VALINE
FMOC-D-VAL
FMOC-D-VALINE
FMOC-D-VAL-OH
N-(9-FLUORENYLMETHOXYCARBONYL)-D-VALINE
N-9-FLUORENYLMETHYLOXYCARBONYL-D-VALINE
N-[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]-D-VALINE
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-VALINE
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-VALINE
N-ALPHA-FMOC-D-VALINE
N-FMOC-D-VALINE
FMOC-D-VALINE 98%
FLUORENYLMETHOXYCARBONYL-D-VALINE(FMOC-D-VAL-OH)
2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-methylbutanoic acid
FMOC-D-VALINE extrapure
N-(9-Fluorenylmethoxycarbonyl)-D-valine, Fmoc-D-valine
Nα-(9-Fluorenylmethyloxycarbonyl)-D-valine ,99% | [EINECS(EC#)]
1533716-785-6 | [Molecular Formula]
C20H21NO4 | [MDL Number]
MFCD00062953 | [Molecular Weight]
339.39 | [MOL File]
84624-17-9.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powde | [Melting point ]
143-144 °C(lit.) | [alpha ]
17 º (c=1, DMF) | [Boiling point ]
551.8±33.0 °C(Predicted) | [density ]
1.229±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C
| [solubility ]
Chloroform (Slightly), DMF (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
3.90±0.10(Predicted) | [color ]
White | [Optical Rotation]
Consistent with structure | [Water Solubility ]
Solubility in methanol (almost transparency). Slightly soluble in water. | [Detection Methods]
T,NMR,Rotation | [BRN ]
6489548 | [CAS DataBase Reference]
84624-17-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [HS Code ]
29242990 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powde | [Uses]
N-Fmoc-D-valine is an N-Fmoc-protected form of D-Valine (V094200). D-Valine (an isomer of the essential amino acid L-Valine [V094205])exhibited inhibitory effects on fibroblasts that contaminated mammalian kidney cultures, allowing for selective growth epithelial cells. D-Valine is also known for its presence in the structure of Actinomycin D, an antitumour drug. D-Valine is naturally synthesized by Streptomyces antibioticus. | [reaction suitability]
reaction type: Fmoc solid-phase peptide synthesis | [Synthesis]
General procedure for the synthesis of Fmoc-D-valine from D-valine and chloroformic acid-9-fluorenylmethyl ester: A 500 mL three-necked flask was taken, and D-valine (4.5 g, 38.9 mmol), dioxane (40 mL), and 10% aqueous sodium carbonate (100 mL) were added sequentially. The reaction system was placed in an ice bath and mechanical stirring was initiated. A dioxane solution (100 mL) of methyl chloroformate-9-fluorenyl (10.0 g, 38.8 mmol) was prepared in a dropping funnel and slowly added dropwise to the reaction vial. After the dropwise addition was completed, it was gradually brought to room temperature and stirring was continued overnight. After completion of the reaction, 100 mL of water was added to the reaction mixture and extracted three times with 50 mL of ether and the organic phase was discarded. The aqueous phase was cooled in an ice bath, and the pH was adjusted to 1 by slowly adding 1 M dilute hydrochloric acid, followed by extracting the aqueous phase with 50 mL ethyl acetate three times, combining the organic phases and drying with anhydrous magnesium sulfate. The desiccant was removed by filtration and the organic phase was concentrated under reduced pressure to give the white solid product Fmoc-D-valine (12.6 g, 96% yield). | [References]
[1] Patent: CN106588987, 2017, A. Location in patent: Paragraph 0172; 0173; 0174
[2] Chemistry - A European Journal, 2014, vol. 20, # 21, p. 6526 - 6531 |
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