2462-32-0

  • Product NameL-Phenylalanine benzyl ester hydrochloride
  • Molecular FormulaC16H17NO2.HCl
  • Molecular Weight291.777
  • Purity99%
  • AppearanceWhite crystalline powder
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Product Details

Quick Details

  • CasNo: 2462-32-0
  • Molecular Formula: C16H17NO2.HCl
  • Appearance: White crystalline powder
  • Purity: 99%

Fast Delivery Pharmaceutical Intermediates L-Phenylalanine benzyl ester hydrochloride 2462-32-0

  • Molecular Formula:C16H17NO2.HCl
  • Molecular Weight:291.777
  • Appearance/Colour:White crystalline powder 
  • Vapor Pressure:4.62E-06mmHg at 25°C 
  • Melting Point:197-200 ºC 
  • Refractive Index:-12 ° (C=1, 80% acetic acid) 
  • Boiling Point:382.8 °C at 760 mmHg 
  • Flash Point:220.4 °C 
  • PSA:52.32000 
  • LogP:3.80210 

L-Phenylalanine benzyl ester hydrochloride(Cas 2462-32-0) Usage

Chemical Properties

White crystal

Uses

L-Phenylalanine Benzyl Ester Hydrochloride is a commonly used reactant for the synthesis of L-isoserine derivatives as aminopeptidase N inhibitors and PF-04449913 as a potent and orally bioavailable inhibitor of smoothened.

InChI:InChI=1/C16H17NO2.ClH/c17-15(11-13-7-3-1-4-8-13)16(18)19-12-14-9-5-2-6-10-14;/h1-10,15H,11-12,17H2;1H/t15-;/m0./s1

2462-32-0 Relevant articles

Fluorinated epoxyketone-based compounds and uses thereof as proteasome inhibitors

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Page/Page column 67, (2016/09/28)

The present application relates to novel...

Chiral recognition of carboxylates by a static library of thiourea receptors with amino acid arms

Ulatowski, Filip,Jurczak, Janusz

, p. 4235 - 4243 (2015/05/13)

Chiral recognition is based on a large n...

Synthesis of a novel series of L-isoserine derivatives as aminopeptidase N inhibitors

Yang, Kanghui,Fen, Jinghong,Fang, Hao,Zhang, Lei,Gong, Jianzhi,Xu, Wenfang

scheme or table, p. 302 - 310 (2012/07/02)

A series of novel L-isoserine derivative...

Design, synthesis and biological evaluation of potent azadipeptide nitrile inhibitors and activity-based probes as promising anti-Trypanosoma brucei agents

Yang, Peng-Yu,Wang, Min,Li, Lin,Wu, Hao,He, Cynthia Y.,Yao, Shao Q.

supporting information; experimental part, p. 6528 - 6541 (2012/07/13)

Trypanosoma cruzi and Trypanosoma brucei...

2462-32-0 Process route

N-(tert-butoxycarbonyl)-L-phenylalanine benzyl ester
66617-58-1

N-(tert-butoxycarbonyl)-L-phenylalanine benzyl ester

L-phenylalanine benzyl ester hydrochloride
2462-32-0

L-phenylalanine benzyl ester hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; In 1,4-dioxane; at 20 ℃; Inert atmosphere;
100%
With hydrogenchloride; In 1,4-dioxane; diethyl ether; at 20 ℃;
76%
With hydrogenchloride; In 1,4-dioxane;
With hydrogenchloride; In ethyl acetate;
With hydrogenchloride; In tetrahydrofuran; 1,4-dioxane; at 0 ℃; for 12h; Inert atmosphere;
hydrochloric acid-dioxane

hydrochloric acid-dioxane

N-(tert-butoxycarbonyl)-L-phenylalanine benzyl ester
66617-58-1

N-(tert-butoxycarbonyl)-L-phenylalanine benzyl ester

L-phenylalanine benzyl ester hydrochloride
2462-32-0

L-phenylalanine benzyl ester hydrochloride

Conditions
Conditions Yield
In diethyl ether; chloroform;
94%

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