77284-32-3

  • Product Name:FMOC-NLE-OH
  • Molecular Formula:C21H23NO4
  • Purity:99%
  • Molecular Weight:353.418
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Product Details;

CAS#: 77284-32-3

Molecular Formula: C21H23NO4

Quality Factory Supply Best Quality 77284-32-3 Customized Supply

  • Molecular Formula:C21H23NO4
  • Molecular Weight:353.418
  • Vapor Pressure:1.25E-13mmHg at 25°C 
  • Melting Point:141-144 °C 
  • Boiling Point:565.6 °C at 760 mmHg 
  • PKA:3.91±0.21(Predicted) 
  • Flash Point:295.9 °C 
  • PSA:75.63000 
  • Density:1.209 g/cm3 
  • LogP:4.55940 

FMOC-NLE-OH(Cas 77284-32-3) Usage

InChI:InChI=1/C21H23NO4/c1-2-3-12-19(20(23)24)22-21(25)26-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,2-3,12-13H2,1H3,(H,22,25)(H,23,24)/p-1/t19-/m1/s1

77284-32-3 Relevant articles

Determination of Chemical and Enantiomeric Purity of α-Amino Acids and their Methyl Esters as N-Fluorenylmethoxycarbonyl Derivatives Using Amylose-derived Chiral Stationary Phases

Islam, Md. Fokhrul,Adhikari, Suraj,Paik, Man-Jeong,Lee, Wonjae

, p. 332 - 338 (2019/04/13)

Liquid chromatographic enantiomer separa...

AMINO ACID ANALOGUES AND METHODS FOR THEIR SYNTHESIS

-

Page/Page column 48-49, (2014/01/18)

A method for the synthesis of an amino a...

Tandem Ru-alkylidene-catalysed cross metathesis/hydrogenation: Synthesis of lipophilic amino acids

Wang, Zhen J.,Spiccia, Nicolas D.,Jackson, W. Roy,Robinson, Andrea J.

, p. 470 - 476 (2013/08/23)

Highly efficient synthesis of lipidic am...

77284-32-3 Process route

Fmoc-norleucine
144701-20-2

Fmoc-norleucine

Fmoc-(S)-2-aminohexanoic acid
77284-32-3,144701-20-2

Fmoc-(S)-2-aminohexanoic acid

(R)-((9H-fluoren-9-yl)methoxy)carbonyl-D-norleucine
112883-41-7,144701-20-2

(R)-((9H-fluoren-9-yl)methoxy)carbonyl-D-norleucine

Conditions
Conditions Yield
With trifluoroacetic acid; In hexane; isopropyl alcohol; at 25 ℃; Reagent/catalyst; Resolution of racemate;
 
(fluorenylmethoxy)carbonyl chloride
28920-43-6

(fluorenylmethoxy)carbonyl chloride

Fmoc-(S)-2-aminohexanoic acid
77284-32-3,144701-20-2

Fmoc-(S)-2-aminohexanoic acid

(R)-((9H-fluoren-9-yl)methoxy)carbonyl-D-norleucine
112883-41-7,144701-20-2

(R)-((9H-fluoren-9-yl)methoxy)carbonyl-D-norleucine

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1.1: sodium carbonate / water; 1,4-dioxane / Cooling with ice
1.2: 5 h / 20 °C
2.1: trifluoroacetic acid / isopropyl alcohol; hexane / 25 °C / Resolution of racemate
With sodium carbonate; trifluoroacetic acid; In 1,4-dioxane; hexane; water; isopropyl alcohol;
 

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