127000-90-2

  • 产品名称:1-(((2R,3S)-2-(2,4-二氟苯基)-3-甲基环氧乙基-2-基)甲基)-1H-1,2,4-三唑
  • 分子式:C12H11F2N3O
  • 纯度:99%
  • 分子量:251.236
询价

产品详情

外观:White or off-white Solid

 

  • Molecular Formula:C12H11F2N3O
  • Molecular Weight:251.236
  • Appearance/Colour:White or off-white Solid 
  • Boiling Point:371.6±52.0 °C(Predicted) 
  • PKA:2.75±0.10(Predicted) 
  • PSA:43.24000 
  • Density:1.41±0.1 g/cm3 (20 oC 760 Torr) 
  • LogP:1.87050 

127000-90-2 Relevant articles

NOVEL METHOD FOR PREPARATION OF EPOXYTRIAZOLE DERIVATIVES

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Paragraph 0109; 0115-0116; 0126-0127, (2021/04/13)

The present invention relates to novel p...

Asymmetric Catalytic Epoxidation of Terminal Enones for the Synthesis of Triazole Antifungal Agents

Feng, Xiaoming,He, Qianwen,Liu, Xiaohua,Zhang, Dong,Zhang, Fengcai

supporting information, p. 6961 - 6966 (2021/09/11)

An enantioselective epoxidation of α-sub...

PROCESS FOR PRODUCING EPOXY ALCOHOL COMPOUND

-

Paragraph 0127, (2020/06/29)

A compound represented by formula (II): ...

Triazole alcohol derivative, and preparation method and application thereof

-

, (2020/05/01)

The invention relates to a triazole alco...

127000-90-2 Process route

(2R,3R)-2-(2,4-difluorophenyl)-3-methanesulfonyloxy-1-(1H-1,2,4-triazol-1-yl)-2-butanol
126945-34-4,132507-78-9,135270-06-3,135270-09-6,135270-12-1,133775-26-5

(2R,3R)-2-(2,4-difluorophenyl)-3-methanesulfonyloxy-1-(1H-1,2,4-triazol-1-yl)-2-butanol

1-(((2R,3S)-2-(2,4-difluorophenyl)-3-methyloxiran-2-yl)-methyl)-1H-1,2,4-triazole
124627-86-7,132563-70-3,132563-77-0,135270-07-4,135270-10-9,135270-13-2,141611-70-3,127000-90-2

1-(((2R,3S)-2-(2,4-difluorophenyl)-3-methyloxiran-2-yl)-methyl)-1H-1,2,4-triazole

Conditions
Conditions Yield
With sodium methylate; In methanol; at 0 ℃; for 0.5h;
81%
With sodium methylate; In methanol; at 0 - 20 ℃; for 0.5h;
72.2%
With sodium methylate; In methanol; at 23 - 28 ℃; for 2h;
60%
With sodium methylate; In methanol; at 0 ℃; for 0.25h; Yield given;
 
With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide; Yield given;
 
With sodium methylate; In methanol; at 0 ℃;
 
(2R,3R)-3-(2,4-difluorophenyl)-3-hydroxy-4-(1H-1,2,4-triazol-1-yl)butane-2-yl dimethyl phosphate

(2R,3R)-3-(2,4-difluorophenyl)-3-hydroxy-4-(1H-1,2,4-triazol-1-yl)butane-2-yl dimethyl phosphate

1-(((2R,3S)-2-(2,4-difluorophenyl)-3-methyloxiran-2-yl)-methyl)-1H-1,2,4-triazole
124627-86-7,132563-70-3,132563-77-0,135270-07-4,135270-10-9,135270-13-2,141611-70-3,127000-90-2

1-(((2R,3S)-2-(2,4-difluorophenyl)-3-methyloxiran-2-yl)-methyl)-1H-1,2,4-triazole

Conditions
Conditions Yield
With sodium methylate; at 23 - 28 ℃; for 2h;
90%
With sodium methylate; In methanol; at 23 - 28 ℃; for 2h;
90%

127000-90-2 Upstream products

  • 132507-89-2
    132507-89-2

    (2R,3S)-2-(2,4-Difluoro-phenyl)-1-[1,2,4]triazol-1-yl-butane-2,3-diol

  • 124-63-0
    124-63-0

    methanesulfonyl chloride

  • 126918-20-5
    126918-20-5

    (2R*,3R*)-2-(2,4-Difluorophenyl)-1,2,3-butanetriol

  • 132563-81-6
    132563-81-6

    1-(2,4-difluorophenyl)-2-(tetrahydropyranyloxy)propan-1-one

127000-90-2 Downstream products

  • 132507-77-8
    132507-77-8

    Trifluoro-acetic acid (1R,2S)-2-(2,4-difluoro-phenyl)-2-hydroxy-1-methyl-3-[1,2,4]triazol-1-yl-propyl ester

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