117142-26-4

  • Product NameBoc-3-(3-pyridyl)-L-alanine
  • Molecular FormulaC13H18N2O4
  • Molecular Weight266.297
  • Purity99%
  • Appearanceoff-white to pale yellow crystalline powder
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Product Details

Quick Details

  • CasNo: 117142-26-4
  • Molecular Formula: C13H18N2O4
  • Appearance: off-white to pale yellow crystalline powder
  • Purity: 99%

High Quality Boc-3-(3-pyridyl)-L-alanine 117142-26-4 Chinese Supplier

  • Molecular Formula:C13H18N2O4
  • Molecular Weight:266.297
  • Appearance/Colour:off-white to pale yellow crystalline powder 
  • Vapor Pressure:5.43E-09mmHg at 25°C 
  • Melting Point:136-142 °C 
  • Refractive Index:1.53 
  • Boiling Point:452.9 °C at 760 mmHg 
  • PKA:3.43±0.10(Predicted) 
  • Flash Point:227.7 °C 
  • PSA:88.52000 
  • Density:1.2 g/cm3 
  • LogP:1.99290 

Boc-3-(3-pyridyl)-L-alanine(Cas 117142-26-4) Usage

Chemical Properties

off-white to pale yellow crystalline powder

Uses Boc-3-(3-pyridyl)-L-alanine is a chemical compound that is commonly used in the field of organic chemistry. It is often used as a building block in the synthesis of complex molecules, such as peptides and natural products. Specifically, Boc-3-(3-pyridyl)-L-alanine is used as an amino acid surrogate in peptide synthesis, due to its ability to form similar secondary structures as the natural amino acid alanine. Additionally, the pyridine moiety in the compound can be used for further functionalization in the synthesis of more complex molecules. The resulting peptides can be used for a variety of applications, such as drug development and biochemical research.

IUPAC Name: (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-pyridin-3-ylpropanoic acid  
Isomeric SMILES: CC(C)(C)OC(=O)N[C@@H](CC1=CN=CC=C1)C(=O)O  
InChIKey: JLBCSWWZSSVXRQ-JTQLQIEISA-N  
InChI: InChI=1S/C13H18N2O4/c1-13(2,3)19-12(18)15-10(11(16)17)7-9-5-4-6-14-8-9/h4-6,8,10H,7H2,1-3H3,(H,15,18)(H,16,17)/t10-/m0/s1  

117142-26-4 Relevant articles

ANTITHROMBOTIC AMIDINOTETRAHYDROPYRIDYLALANINE DERIVATIVES

-

, (2008/06/13)

This invention is directed to compounds ...

117142-26-4 Process route

di-<i>tert</i>-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

(S)-2-tert-butoxycarbonylamino-3-pyridin-3-yl-propionic acid
117142-26-4,105454-25-9

(S)-2-tert-butoxycarbonylamino-3-pyridin-3-yl-propionic acid

Conditions
Conditions Yield
With sodium chloride; potassium carbonate; citric acid; In 1,4-dioxane; water;
72%
(S)-2-tert-butoxycarbonylamino-3-pyridin-3-yl-propionic acid
117142-26-4,105454-25-9

(S)-2-tert-butoxycarbonylamino-3-pyridin-3-yl-propionic acid

N-t-Butoxycarbonyl-3-(pyridin-3-yl)-(S)-alanine t-butyl ester
184879-69-4

N-t-Butoxycarbonyl-3-(pyridin-3-yl)-(S)-alanine t-butyl ester

Conditions
Conditions Yield
 
100%

117142-26-4 Upstream products

  • 24424-99-5
    24424-99-5

    di-tert-butyl dicarbonate

117142-26-4 Downstream products

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    C20H24N2O4

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    Benzyl [N2-(tert-butoxycarbonyl)-3-(3-pyridyl)-L-alanyl]-L-serinate

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    1184867-79-5

    C36H39N5O5S

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    C33H46N6O6

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