71989-28-1

  • Product Name:Fmoc-L-Methionine
  • Molecular Formula:C20H21NO4S
  • Purity:99%
  • Molecular Weight:371.457
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Product Details;

CAS#: 71989-28-1

Molecular Formula: C20H21NO4S

Appearance: white to light yellow crystal powder

Factory Supply High Purity Top Purity ≥99.5% 71989-28-1 with Safe Transportation

  • Molecular Formula:C20H21NO4S
  • Molecular Weight:371.457
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:5.8E-16mmHg at 25°C 
  • Melting Point:121-123 °C(lit.) 
  • Refractive Index:-29.5 ° (C=1, DMF) 
  • Boiling Point:614.6 °C at 760 mmHg 
  • PKA:3.72±0.10(Predicted) 
  • Flash Point:325.5 °C 
  • PSA:100.93000 
  • Density:1.282 g/cm3 
  • LogP:4.12230 

Fmoc-L-Methionine(Cas 71989-28-1) Usage

InChI:InChI=1/C20H21NO4S/c1-26-11-10-18(19(22)23)21-20(24)25-12-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,10-12H2,1H3,(H,21,24)(H,22,23)/p-1/t18-/m0/s1

71989-28-1 Relevant articles

Diethyl Selenodiglycolate: An Eco-Friendly Synthetic Antioxidant with Potential Application to Inflammatory Disorders

Archilha, Marcos V. L. R.,Giroldo, Lilian,Kuznetsov, Aleksey E.,Meotti, Flávia C.,Pinatto-Botelho, Marcos F.,da Silva, Railmara P.,dos Santos, Alcindo A.

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This study describes a single step, high...

Novel chiral stationary phases based on 3,5-dimethyl phenylcarbamoylated β-cyclodextrin combining cinchona alkaloid moiety

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, p. 1080 - 1090 (2020/05/25)

Novel chiral selectors based on 3,5-dime...

Repurposing the Pummerer Rearrangement: Determination of Methionine Sulfoxides in Peptides

Woodroofe, Carolyn C.,Ivanic, Joseph,Monti, Sarah,Levine, Rodney L.,Swenson, Rolf E.

, p. 508 - 516 (2019/11/13)

The reversible oxidation of methionine r...

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...

71989-28-1 Process route

L-methionine
63-68-3,26062-47-5,58576-49-1

L-methionine

(fluorenylmethoxy)carbonyl chloride
28920-43-6

(fluorenylmethoxy)carbonyl chloride

N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-methionine
71989-28-1

N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-methionine

Conditions
Conditions Yield
L-methionine; With chloro-trimethyl-silane; In dichloromethane; for 1h; Inert atmosphere; Reflux;
(fluorenylmethoxy)carbonyl chloride; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 5 - 20 ℃; for 1.5h;
80%
In acetonitrile; at 20 ℃; for 0.25h; pH=9.2; aq. borate buffer;
 
L-methionine; With sodium carbonate; In 1,4-dioxane; water; Cooling with ice;
(fluorenylmethoxy)carbonyl chloride; In 1,4-dioxane; water; at 20 ℃; for 5h;
 
L-methionine
63-68-3,26062-47-5,58576-49-1

L-methionine

N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide
82911-69-1

N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide

N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-methionine
71989-28-1

N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-methionine

Conditions
Conditions Yield
With sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 50 ℃;
78%
L-methionine; With N-cyclohexyl-cyclohexanamine; In acetone; at 20 ℃;
N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide; With sodium carbonate; In water; acetonitrile; at 0 - 20 ℃; pH=8;
With potassium hydrogensulfate; In water; acetonitrile; pH=2 - 3;
61%
With sodium hydrogencarbonate; In water; N,N-dimethyl-formamide; at 0 - 20 ℃; for 2h;
 

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