FMOC-PHE-OL
FMOC-PHE-OL Basic information
- Product Name:
- FMOC-PHE-OL
- Synonyms:
-
- N-FMOC-L-PHENYLALANINOL
- N-ALPHA-FMOC-L-PHENYLALANINOL
- N-(9-FLUORENYLMETHOXYCARBONYL)-L-PHENYLALANINOL
- FMOC-L-PHENYLALANINOL
- FMOC-PHENYLALANINOL
- FMOC-PHE-OL
- FMOC-(S)-2-AMINO-3-PHENYL-1-PROPANOL
- Fmoc-DL-Phenylalaninol
- CAS:
- 129397-83-7
- MF:
- C24H23NO3
- MW:
- 373.44
- Product Categories:
-
- Amino Alcohols
- Fmoc-Amino acid series
- Amino Acids
- peptides
- Mol File:
- 129397-83-7.mol
FMOC-PHE-OL Chemical Properties
- Melting point:
- 129-130 °C
- Boiling point:
- 606.1±50.0 °C(Predicted)
- Density
- 1.219±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,2-8°C
- solubility
- Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
- pka
- 11.44±0.46(Predicted)
- form
- Solid
- Appearance
- White to off-white Solid
- CAS DataBase Reference
- 129397-83-7(CAS DataBase Reference)
Safety Information
- Safety Statements
- 24/25
- HazardClass
- IRRITANT
- HS Code
- 29051990
FMOC-PHE-OL Usage And Synthesis
Chemical Properties
White to off-white powder
Synthesis
35661-40-6
129397-83-7
The general procedure for the synthesis of Fmoc-L-phenylalaninol from Fmoc-L-phenylalanine was as follows: Fmoc-L-phenylalanine (10 mmol) was dissolved in THF (10 mL) at 0 °C, followed by the sequential addition of DIPEA (11 mmol, 1.42 mL) and EtOAc solution of 50% T3P (20 mmol, 6.36 mL). The reaction mixture was stirred at this temperature for about 10 minutes. Next, aqueous NaBH4 solution (10 mmol, 388 mg, dissolved in 0.3 mL H2O) was slowly added to the reaction system at the same temperature. The reaction progress was monitored by TLC until the reaction was complete. After completion of the reaction, the solvent was removed by rotary evaporation and the crude product was extracted with EtOAc. The organic phase was washed sequentially with 5% citric acid solution (10 mL × 2), 5% Na2CO3 solution (10 mL × 2), water and saturated saline. Finally, the organic phase was dried over anhydrous Na2SO4 and concentrated under reduced pressure to obtain the target product Fmoc-L-phenylalaninol.
References
[1] Tetrahedron Letters, 2012, vol. 53, # 38, p. 5059 - 5063
[2] Journal of Organic Chemistry, 2001, vol. 66, # 25, p. 8454 - 8462
[3] Tetrahedron Letters, 2000, vol. 41, # 32, p. 6131 - 6135
[4] Organic Letters, 2008, vol. 10, # 10, p. 1881 - 1884
[5] Tetrahedron Letters, 1999, vol. 40, # 23, p. 4395 - 4396
FMOC-PHE-OLSupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
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- 5108538618
- suger.wang@chemfuture.com
- Tel
- 21-61263452 13641803416
- ymbetter@glbiochem.com
- Tel
- +86 (0) 571 85 58 67 18
FMOC-PHE-OL(129397-83-7)Related Product Information
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- FMOC-D-ORN(BOC)-OH
- FMOC-D-TRP(ME)-OH
- Fmoc-Tyr(tBu)-OH
- Fmoc-O-benzyl-L-tyrosine
- Fmoc-N-methyl-L-phenylalanine
- FMOC-PHE-OH
- FMOC-TYR(2-BR-Z)-OH
- FMOC-D-4-Chlorophe
- Fmoc-4-nitro-L-phenylalanine
- Nalpha-Fmoc-L-tyrosine
- FMOC-TIC-OH
- (S)-N-Fmoc-1-Naphthylalanine
- FMOC-3,5-DIIODO-L-TYROSINE
- FMOC-2-NAL-OH
- FMOC-PHE-OL 99+%,FMOC-PHE-OL 98+%
- L-Phenylglycinol
- DL-PHENYLALANINOL