95753-56-3
- Product Name：Fmoc-L-Phe(4-NH2)-OH
- Molecular Formula：C24H22N2O4
- Purity：99%
- Molecular Weight：402.45
Product Details;
CasNo： 95753-56-3
Molecular Formula： C24H22N2O4
99% Purity Commercial production Fmoc-L-Phe(4-NH2)-OH 95753-56-3 with Cheapest Price
- Molecular Formula:C24H22N2O4
- Molecular Weight:402.45
- Boiling Point:671.5 °C at 760 mmHg
- PKA:3.63±0.10(Predicted)
- Flash Point:359.9 °C
- PSA：101.65000
- Density:1.316 g/cm3
- LogP:4.77530
Fmoc-4-Amino-L-phenylalanine(Cas 95753-56-3) Usage
InChI:InChI=1/C24H22N2O4/c25-16-11-9-15(10-12-16)13-22(23(27)28)26-24(29)30-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22H,13-14,25H2,(H,26,29)(H,27,28)/t22-/m0/s1
95753-56-3 Relevant articles
Synthesis of new tetrazolyl derivatives of L- and D-phenylalanine
Tolstyakov,Tolstobrova,Zarubina,Popova,Protas,Chuprun,Trifonov
, p. 1681 - 1685 (2017/01/28)
New tetrazolyl derivatives of L- and D-p...
Incorporation of non-natural amino acids improves cell permeability and potency of specific inhibitors of proteasome trypsin-like sites
Geurink, Paul P.,Van Der Linden, Wouter A.,Mirabella, Anne C.,Gallastegui, Nerea,De Bruin, Gerjan,Blom, Annet E. M.,Voges, Mathias J.,Mock, Elliot D.,Florea, Bogdan I.,Van Der Marel, Gijs A.,Driessen, Christoph,Van Der Stelt, Mario,Groll, Michael,Overkleeft, Herman S.,Kisselev, Alexei F.
supporting information, p. 1262 - 1275 (2013/03/29)
Proteasomes degrade the majority of prot...
N-alkanoylphenylalanine derivatives
-
, (2008/06/13)
Compounds of the formula: are disclosed ...
N-aroylphenylalanine derivative VCAM-1 inhibitors
-
, (2008/06/13)
Compounds of the formula: are disclosed ...
95753-56-3 Process route
-
-
95753-55-2,177966-63-1
N-α-FMOC-4-nitro-L-phenylalanine
-
![4-amino-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine](/upload/2026/7/80856997-4360-42d6-9bd7-31f4c29c12e9.png)
-
95753-56-3,324017-21-2
4-amino-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
| Conditions | Yield |
|---|---|
|
With
hydrogen;
palladium on activated charcoal;
In
ethanol;
for 1h;
|
93% |
|
With
hydrogen;
palladium on activated charcoal;
In
1,4-dioxane;
for 1h;
Ambient temperature;
|
90% |
|
With
hydrogen;
palladium on activated charcoal;
In
methanol;
under 760 Torr;
|
|
|
With
palladium 10% on activated carbon; ammonium formate;
In
methanol;
at 20 ℃;
for 14h;
|
|
|
Multi-step reaction with 2 steps
1: hydrogenchloride; zinc / water; isopropyl alcohol
2: hydrogenchloride; water / 6 h / Reflux
With
hydrogenchloride; water; zinc;
In
water; isopropyl alcohol;
|
-
-
95753-55-2,177966-63-1
N-α-FMOC-4-nitro-L-phenylalanine
-
![isopropyl ether of N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-amino-L-phenylalanine](/upload/2026/7/3566988c-08cd-4864-a531-bfdd66a5e982.png)
-
isopropyl ether of N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-amino-L-phenylalanine
-
-
95753-56-3,324017-21-2
4-amino-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride; zinc;
In
water; isopropyl alcohol;
|
95753-56-3 Upstream products
-
95753-55-2
N-α-FMOC-4-nitro-L-phenylalanine
-
943-80-6
4-amino-L-phenylalanine
-
82911-69-1
N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide
-
949-99-5
4-nitro-3-phenyl-L-alanine
95753-56-3 Downstream products
-
95753-57-4
N-Fmoc-L-p-aminophenylalanine methyl ester hydrochloride
-
197724-51-9
(E)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(phenyldiazenyl)phenyl)propanoic acid
-
88576-96-9
Fmoc-L-p-isothiocyanophenylalanine methyl ester
-
95753-63-2
DL-5-isopropyl-3-<4-<(2S)-Fmocamino-2-methoxycarbonylethyl>phenyl>-2-thiohydantoin
Relevant Products
-
Fmoc-2-Nal-OHCAS：112883-43-9
-
Eicosanedioic AcidCAS：2424-92-2
-
16-(tert-butoxy)-16-oxohexadecanoic acidCAS：843666-27-3
