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2163-11-3

2163-11-3

Identification

  • Product Name:Ethanol, 2-[2-[(tetrahydro-2H-pyran-2-yl)oxy]ethoxy]-

  • CAS Number: 2163-11-3

  • EINECS:

  • Molecular Weight:190.24

  • Molecular Formula: C9H18O4

  • HS Code:2932999099

  • Mol File:2163-11-3.mol

Synonyms:2-[2-(oxan-2-yloxy)ethoxy]ethanol;

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  • Manufacture/Brand:TRC
  • Product Description:Tetrahydropyranyldiethyleneglycol
  • Packaging:250mg
  • Price:$ 130
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  • Manufacture/Brand:Medical Isotopes, Inc.
  • Product Description:Tetrahydropyranyldiethyleneglycol
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  • Manufacture/Brand:Matrix Scientific
  • Product Description:Tetrahydropyranyldiethyleneglycol 95%
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  • Manufacture/Brand:BroadPharm
  • Product Description:THP-PEG3 95%
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  • Product Description:THP-PEG3 95%
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  • Manufacture/Brand:BroadPharm
  • Product Description:THP-PEG3 95%
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  • Manufacture/Brand:American Custom Chemicals Corporation
  • Product Description:TETRAHYDROPYRANYLDIETHYLENEGLYCOL 95.00%
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  • Manufacture/Brand:Acrotein
  • Product Description:THP-PEG2-OH 97%
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  • Manufacture/Brand:Acrotein
  • Product Description:THP-PEG2-OH 97%
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  • Manufacture/Brand:Acrotein
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Relevant articles and documentsAll total 15 Articles be found

PYRROLO[2,3-B]PYRIDIN DERIVATIVES AS INHIBITORS OF INFLUENZA VIRUS REPLICATION

-

Paragraph 00271, (2020/02/16)

Provided herein are compounds of Formula A, B or C that can inhibit the replication of influenza viruses, reduce the amount of influenza viruses, and/or treat influenza.

PYRROLOPYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF INFLUENZA VIRUS REPLICATION

-

Paragraph 00290, (2018/11/22)

Methods of inhibiting the replication of influenza viruses in a biological sample or patient, of reducing the amount of influenza viruses in a biological sample or patient, and of treating influenza in a patient, comprises administering to said biological sample or patient a safe and effective amount of a compound represented by any of Formulas l-lll, or a pharmaceutically acceptable salt thereof. A pharmaceutical composition comprises a safe and effective amount of such a compound or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, adjuvant or vehicle.

DIAGNOSTIC AGENT FOR THERAPEUTIC EFFECT ON CANCER

-

Paragraph 0078; 0079; 0080, (2016/09/26)

The present invention provides a diagnostic agent for a therapeutic effect on cancer, containing a compound represented by formula (1-0). (In formula (1-0), R represents —O(CH2)n—, —O(CH2)nOC2H4—, —CH2O(CH2)n—, or —CH2O(CH2)nOC2H4—, n represents an integer of 1 to 5, and Q1 represents F or —OCH3.)

INHIBITORS OF HEPATITIS C VIRUS POLYMERASE

-

Paragraph 231; 234, (2016/10/11)

The present invention provides, among other things, compounds represented by the general Formula I: (I) and pharmaceutically acceptable salts thereof, wherein L and A (and further substituents) are as defined in classes and subclasses herein and compositions (e.g., pharmaceutical compositions) comprising such compounds, which compounds are useful as inhibitors of hepatitis C virus polymerase, and thus are useful, for example, as medicaments for the treatment of HCV infection.

P-stereogenic diphosphacrowns: Facile incorporation of aromatic rings

Kato, Ryosuke,Watanabe, Hiroyuki,Morisaki, Yasuhiro,Chujo, Yoshiki

, (2016/03/01)

P-Stereogenic diphosphacrowns containing naphthalene and pyridine rings were synthesized. Facile incorporation of aromatic rings, and chains of different lengths, into the diphosphacrown skeleton was achieved by altering the electrophile in our previously

Process route upstream and downstream products

Process route

3,4-dihydro-2<i>H</i>-pyran
110-87-2

3,4-dihydro-2H-pyran

diethylene glycol
111-46-6

diethylene glycol

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol
2163-11-3

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol

Conditions
Conditions Yield
With toluene-4-sulfonic acid; at -10 - 20 ℃; for 3h; Inert atmosphere;
70%
With toluene-4-sulfonic acid; at 0 - 20 ℃; for 26.5h;
69%
With pyridinium p-toluenesulfonate; In chloroform; for 24h; Ambient temperature;
60%
With toluene-4-sulfonic acid; In dichloromethane; at 0 ℃;
57%
diethylene glycol; With toluene-4-sulfonic acid; In dichloromethane; at 20 ℃; for 0.5h;
3,4-dihydro-2H-pyran; In dichloromethane; at 80 ℃; for 10h;
50%
With pyridinium p-toluenesulfonate; In chloroform; at 20 ℃; Inert atmosphere;
42%
With toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; at -10 ℃; for 1h;
31%
With toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; at -10 ℃; for 1h;
31%
With toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; at -10 ℃; for 1h;
31%
With toluene-4-sulfonic acid; In dichloromethane; at 0 ℃; for 4h;
30%
With pyridinium p-toluenesulfonate; In dichloromethane; at 0 - 20 ℃; for 4h;
17%
With pyridinium p-toluenesulfonate; In dichloromethane; at 0 - 20 ℃; for 4h;
17%
With toluene-4-sulfonic acid; In dichloromethane;
TETRAHYDROPYRANE
142-68-7

TETRAHYDROPYRANE

diethylene glycol
111-46-6

diethylene glycol

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol
2163-11-3

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol

Conditions
Conditions Yield
With toluene-4-sulfonic acid; In dichloromethane; at 0 ℃;
57%
With pyridinium p-toluenesulfonate; In dichloromethane;
53%
2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol
2163-11-3

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol

Conditions
Conditions Yield
3,4-dihydro-2<i>H</i>-pyran
110-87-2

3,4-dihydro-2H-pyran

diethylene glycol
111-46-6

diethylene glycol

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol
2163-11-3

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol

Conditions
Conditions Yield
With toluene-4-sulfonic acid; at -10 - 20 ℃; for 3h; Inert atmosphere;
70%
With toluene-4-sulfonic acid; at 0 - 20 ℃; for 26.5h;
69%
With pyridinium p-toluenesulfonate; In chloroform; for 24h; Ambient temperature;
60%
With toluene-4-sulfonic acid; In dichloromethane; at 0 ℃;
57%
diethylene glycol; With toluene-4-sulfonic acid; In dichloromethane; at 20 ℃; for 0.5h;
3,4-dihydro-2H-pyran; In dichloromethane; at 80 ℃; for 10h;
50%
With pyridinium p-toluenesulfonate; In chloroform; at 20 ℃; Inert atmosphere;
42%
With toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; at -10 ℃; for 1h;
31%
With toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; at -10 ℃; for 1h;
31%
With toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; at -10 ℃; for 1h;
31%
With toluene-4-sulfonic acid; In dichloromethane; at 0 ℃; for 4h;
30%
With pyridinium p-toluenesulfonate; In dichloromethane; at 0 - 20 ℃; for 4h;
17%
With pyridinium p-toluenesulfonate; In dichloromethane; at 0 - 20 ℃; for 4h;
17%
With toluene-4-sulfonic acid; In dichloromethane;
TETRAHYDROPYRANE
142-68-7

TETRAHYDROPYRANE

diethylene glycol
111-46-6

diethylene glycol

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol
2163-11-3

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol

Conditions
Conditions Yield
With toluene-4-sulfonic acid; In dichloromethane; at 0 ℃;
57%
With pyridinium p-toluenesulfonate; In dichloromethane;
53%
2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol
2163-11-3

2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol

Conditions
Conditions Yield

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  • Finetech Industry Limited
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  • SAGECHEM LIMITED
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  • Emails:will@sagechem.com
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  • Country:China (Mainland)
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