17342-08-4

  • Product NameL-Pyroglutaminol
  • Molecular FormulaC5H9NO2
  • Molecular Weight115.132
  • Purity99%
  • Appearancewhite to light yellow crystals or crystalline powder
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Product Details

Quick Details

  • CasNo: 17342-08-4
  • Molecular Formula: C5H9NO2
  • Appearance: white to light yellow crystals or crystalline powder
  • Purity: 99%

Pharmaceutical Intermediates L-Pyroglutaminol 17342-08-4 Crystalline Powder

  • Molecular Formula:C5H9NO2
  • Molecular Weight:115.132
  • Appearance/Colour:white to light yellow crystals or crystalline powder 
  • Melting Point:79-80 °C(lit.) 
  • Refractive Index:31 ° (C=5, EtOH) 
  • Boiling Point:346 °C at 760 mmHg 
  • PKA:14.35±0.10(Predicted) 
  • Flash Point:163 °C 
  • PSA:49.33000 
  • Density:1.153 g/cm3 
  • LogP:-0.41390 

L-Pyroglutaminol(Cas 17342-08-4) Usage

Chemical Properties

white to light yellow crystals or

Uses

(S)-Pyroglutaminol (cas# 17342-08-4) is a compound useful in organic synthesis.

17342-08-4 Relevant articles

INHIBITORS OF APOL1 AND METHODS OF USING SAME

-

Paragraph 00307, (2020/07/14)

The disclosure provides at least one ent...

N-Heterocyclic carbene triazolium salts containing brominated aromatic motifs: Features and synthetic protocol

Raed, Anas Abo,Dhayalan, Vasudevan,Barkai, Shahar,Milo, Anat

, p. 878 - 882 (2020/12/25)

In this work, we provide a brief overvie...

Biphenyl compound as well as preparation method and medical application thereof

-

Paragraph 1517-1523, (2020/11/22)

The invention discloses a biphenyl compo...

Practical Synthesis of Chiral N-Heterocyclic Carbene Triazolium Salts Containing a Hydroxy Functional Handle

Dhayalan, Vasudevan,Mal, Kanchan,Milo, Anat

, p. 2845 - 2864 (2019/07/04)

A library of functionalized chiral pyrro...

17342-08-4 Process route

ethyl (S)-pyroglutamate
7149-65-7

ethyl (S)-pyroglutamate

(S)-Pyroglutaminol
17342-08-4

(S)-Pyroglutaminol

Conditions
Conditions Yield
With potassium borohydride; lithium chloride; In tetrahydrofuran; at -15 - 20 ℃; for 2h; Reagent/catalyst;
95%
With lithium borohydride; In tetrahydrofuran; at 20 ℃; for 48h;
90%
With sodium tetrahydroborate; In ethanol;
83%
With sodium tetrahydroborate; ethanol; at 0 - 20 ℃; for 6h;
83%
With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 5 ℃; for 1h;
80%
With lithium borohydride; In tetrahydrofuran; for 16h; Ambient temperature;
78%
With sodium tetrahydroborate; ethanol; at 0 - 5 ℃;
78%
With sodium tetrahydroborate; lithium chloride; In tetrahydrofuran; ethanol; at 20 ℃; for 15h;
73%
With sodium tetrahydroborate; lithium chloride; Yield given. Multistep reaction; 1) diglyme, THF, 20 min.; 2) 9h, room temp., THF;
With lithium borohydride; In tetrahydrofuran; dichloromethane; for 2h; Ambient temperature;
With sodium tetrahydroborate; In water; for 1.5h; Ambient temperature;
With sodium tetrahydroborate; In ethanol; at 0 - 20 ℃; for 1.5h;
31.2 g
ethyl (S)-pyroglutamate; With sodium tetrahydroborate; In water; at 20 ℃;
In water; acetone; at 0 ℃;
With sodium tetrahydroborate; In ethanol; at 20 ℃; for 22h;
With sodium tetrahydroborate; ethanol; lithium chloride; In tetrahydrofuran;
With sodium tetrahydroborate; In ethanol; at 20 ℃; for 48h;
With sodium tetrahydroborate; In ethanol;
ethyl (S)-pyroglutamate; With sodium tetrahydroborate; In ethanol; at 10 - 12 ℃; for 17h;
With hydrogenchloride; In ethanol; water; pH=~ 3;
ethyl (S)-pyroglutamate; With sodium tetrahydroborate; In ethanol; at 0 - 20 ℃;
With acetic acid; In ethanol; at 0 - 20 ℃; for 0.5h;
methyl (S)-pyroglutamate
4931-66-2

methyl (S)-pyroglutamate

(S)-Pyroglutaminol
17342-08-4

(S)-Pyroglutaminol

Conditions
Conditions Yield
With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 5 ℃; for 1h;
99%
With sodium tetrahydroborate; In ethanol;
99%
With sodium tetrahydroborate; In ethanol;
99%
With sodium tetrahydroborate; ethanol;
99%
With sodium tetrahydroborate; isopropyl alcohol; at 20 ℃; for 20h;
98%
With sodium tetrahydroborate; In ethanol;
94%
With sodium tetrahydroborate; In ethanol;
93%
With sodium tetrahydroborate; In ethanol; at 0 - 20 ℃;
91%
With sodium tetrahydroborate; In isopropyl alcohol; at 20 ℃; for 20h;
87%
With sodium tetrahydroborate; In isopropyl alcohol; at 20 ℃; for 20h;
86%
With sodium tetrahydroborate; In ethanol; for 2h; Ambient temperature;
85%
With sodium tetrahydroborate; ethanol; at 0 - 20 ℃; for 24h;
84%
With sodium tetrahydroborate; In ethanol; at 20 ℃; for 3h;
82.9%
With sodium tetrahydroborate; In ethanol; at 20 ℃; for 3h;
81%
With sodium tetrahydroborate; In ethanol; at 0 - 20 ℃; Inert atmosphere;
80%
With lithium borohydride; In methanol; Ambient temperature;
80%
With sodium tetrahydroborate; In ethanol; for 2h; Ambient temperature;
78%
With sodium tetrahydroborate; In ethanol; for 2h; Ambient temperature;
75%
With sodium tetrahydroborate; In ethanol;
71%
With sodium tetrahydroborate; ethanol; at 20 ℃; for 2h;
70%
With sodium tetrahydroborate; In ethanol; for 4h; Ambient temperature;
60%
With sodium tetrahydroborate; In ethanol; at 20 ℃; for 2h; Inert atmosphere; Cooling with ice;
59%
With sodium tetrahydroborate; ethanol; at 20 ℃; Cooling with ice;
59%
With sodium tetrahydroborate; In ethanol; at 0 - 20 ℃; Inert atmosphere;
53%
With sodium tetrahydroborate; Yield given;
With sodium tetrahydroborate;
With sodium tetrahydroborate; ethanol; at 0 ℃; for 12h;
With sodium tetrahydroborate; In tetrahydrofuran; methanol; for 1h;
With sodium tetrahydroborate; In ethanol;
With sodium tetrahydroborate; In ethanol; at 0 - 20 ℃; for 18h;
11.5 g
With lithium borohydride; In tetrahydrofuran; at 10 - 40 ℃; for 5h;
With sodium tetrahydroborate; In ethanol; at 20 ℃;
3.3 g
With sodium tetrahydroborate; In ethanol; at 20 ℃;
With sodium tetrahydroborate; In ethanol; at 20 ℃; Cooling with ice; Inert atmosphere;
With sodium tetrahydroborate; In ethanol; at 0 - 20 ℃; for 24h; Inert atmosphere; Schlenk technique;
15 g
With sodium tetrahydroborate; In tetrahydrofuran; methanol; for 8h; Cooling with ice;
3.8 g

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