71989-16-7

  • Product Name:Nalpha-FMOC-L-Asparagine
  • Molecular Formula:C19H18N2O5
  • Purity:99%
  • Molecular Weight:354.362
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Product Details;

CAS#: 71989-16-7

Molecular Formula: C19H18N2O5

Appearance: white to light yellow crystal powder

Factory Supply High Purity 71989-16-7 with Cheapest Price

  • Molecular Formula:C19H18N2O5
  • Molecular Weight:354.362
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:2.43E-19mmHg at 25°C 
  • Melting Point:190 °C (dec.)(lit.) 
  • Refractive Index:-13 ° (C=1, DMF) 
  • Boiling Point:678.6 °C at 760 mmHg 
  • PKA:3.68±0.10(Predicted) 
  • Flash Point:364.2 °C 
  • PSA:118.72000 
  • Density:1.362 g/cm3 
  • LogP:2.94490 

Nalpha-FMOC-L-Asparagine(Cas 71989-16-7) Usage

InChI:InChI=1/C19H18N2O5/c20-17(22)9-16(18(23)24)21-19(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H2,20,22)(H,21,25)(H,23,24)/p-1/t16-/m0/s1

71989-16-7 Relevant articles

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

Zhu, Lunan,Zhu, Junchen,Sun, Xiaotong,Wu, Yaling,Wang, Huiying,Cheng, Lingping,Shen, Jiawei,Ke, Yanxiong

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

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

Optimized syntheses of Fmoc azido amino acids for the preparation of azidopeptides

Pícha, Jan,Budě?ínsky, Milo?,Machá?ková, Kate?ina,Collinsová, Michaela,Jirá?ek, Ji?í

, p. 202 - 214 (2017/04/06)

The rise of CuI-catalyzed click chemistr...

New TFA-free cleavage and final deprotection in Fmoc solid-phase peptide synthesis: Dilute HCl in fluoro alcohol

Palladino, Pasquale,Stetsenko, Dmitry A.

supporting information, p. 6346 - 6349 (2013/02/25)

A novel method for cleaving from resin a...

Liquid-chromatography quantitative analysis of 20 amino acids after derivatization with FMOC-CI and its application to different origin Radix isatidis

Zhou, Wei,Zhang, Xiao-Yan,Duan, Geng-Li

experimental part, p. 509 - 515 (2012/01/04)

We developed a simple, rapid and reliabl...

71989-16-7 Process route

L-asparagine
70-47-3,28088-48-4,7006-34-0

L-asparagine

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

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

Fmoc-Asn-OH
71989-16-7

Fmoc-Asn-OH

Conditions
Conditions Yield
With sodium carbonate; In 1,4-dioxane; water; at 0 - 20 ℃;
87%
L-asparagine; 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;
59%
L-asparagine
70-47-3,28088-48-4,7006-34-0

L-asparagine

(9-fluorenyl)methyl pentafluorophenyl carbonate
88744-04-1

(9-fluorenyl)methyl pentafluorophenyl carbonate

Fmoc-Asn-OH
71989-16-7

Fmoc-Asn-OH

Conditions
Conditions Yield
With sodium hydrogencarbonate; In water; acetone; Ambient temperature;
83%

71989-16-7 Upstream products

  • 70-47-3
    70-47-3

    L-asparagine

  • 88744-04-1
    88744-04-1

    (9-fluorenyl)methyl pentafluorophenyl carbonate

  • 132388-59-1
    132388-59-1

    L-Asn(Trt)

  • 82911-69-1
    82911-69-1

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

71989-16-7 Downstream products

  • 71989-17-8
    71989-17-8

    Nα-fluorenylmethoxycarbonyl-L-asparagine p-nitrophenyl ester

  • 86060-99-3
    86060-99-3

    N-α-Fmoc-L-asparagine pentafluorophenyl ester

  • 126402-76-4
    126402-76-4

    [(S)-3-Carbamoyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-acetic acid benzhydryl ester

  • 200066-58-6
    200066-58-6

    {5-[(S)-3-Carbamoyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-pentyl}-carbamic acid tert-butyl ester

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