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915086-32-7

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  • 4-(3-(4-hydroxyphenyl)-4,4-diMethyl-5-oxo-2-thioxoiMidazolidin-1-yl)-2-(trifluoroMethyl)benzonitrile 915086-32-7

    Cas No: 915086-32-7

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  • Benzonitrile, 4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-thioxo-1-imidazolidinyl]-2-(trifluoromethyl)- cas no. 915086-32-7 98%

    Cas No: 915086-32-7

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915086-32-7 Usage

General Description

The chemical 4-(3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile is a compound with a complex structure containing a benzene ring with a nitrile group attached to it. It also contains a thioxoimidazolidin-1-yl group and a hydroxyphenyl group, both of which are connected to the benzene ring. Additionally, the compound has a trifluoromethyl group attached to the benzene ring. This chemical may have various applications, including pharmaceuticals, agrochemicals, or material science, but would require further investigation and research to fully understand its potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 915086-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,0,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 915086-32:
(8*9)+(7*1)+(6*5)+(5*0)+(4*8)+(3*6)+(2*3)+(1*2)=167
167 % 10 = 7
So 915086-32-7 is a valid CAS Registry Number.

915086-32-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzonitrile, 4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-thioxo-1-imidazolidinyl]-2-(trifluoromethyl)-

1.2 Other means of identification

Product number -
Other names 4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:915086-32-7 SDS

915086-32-7Synthetic route

2-trifluoromethyl-4-[3-(4-hydroxyphenyl)-5-imino-4,4-dimethyl-2-sulfanylideneimidazolidin-1-yl]benzonitrile

2-trifluoromethyl-4-[3-(4-hydroxyphenyl)-5-imino-4,4-dimethyl-2-sulfanylideneimidazolidin-1-yl]benzonitrile

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With hydrogenchloride; water In methanol for 2h; Heating / reflux;98%
With hydrogenchloride; water In methanol for 2h; Reflux; Inert atmosphere;98%
With hydrogenchloride; water In methanol at 100℃; for 2h;93%
2-((4-hydroxyphenyl)amino)-2-methylpropanenitrile
26850-26-0

2-((4-hydroxyphenyl)amino)-2-methylpropanenitrile

4-isothiocyanato 2-(trifluoromethyl)benzonitrile
143782-23-4

4-isothiocyanato 2-(trifluoromethyl)benzonitrile

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
In N,N-dimethyl acetamide at 60℃; for 1.5h; Inert atmosphere;92.9%
Stage #1: 2-((4-hydroxyphenyl)amino)-2-methylpropanenitrile; 4-isothiocyanato 2-(trifluoromethyl)benzonitrile In N,N-dimethyl acetamide at 60℃; for 1.5h;
Stage #2: With hydrogenchloride; water In methanol; N,N-dimethyl acetamide at 20 - 30℃;
92.9%
C13H20N2OSi

C13H20N2OSi

4-isothiocyanato 2-(trifluoromethyl)benzonitrile
143782-23-4

4-isothiocyanato 2-(trifluoromethyl)benzonitrile

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With hydrogenchloride In methanol; N,N-dimethyl acetamide at 15℃; Reflux; Industrial scale;62.3%
4-[3-(4-benzyloxyphenyl)-4,4-dimethyl-5-oxo-2-thioxo-imidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

4-[3-(4-benzyloxyphenyl)-4,4-dimethyl-5-oxo-2-thioxo-imidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With boron tribromide In dichloromethane at -78℃; for 1.5h; Inert atmosphere;92%
4-amino-phenol
123-30-8

4-amino-phenol

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 12 h / Inert atmosphere
2: N,N-dimethyl acetamide / 1.5 h / 60 °C / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 12 h / 20 - 30 °C
2.1: N,N-dimethyl acetamide / 1.5 h / 60 °C
2.2: 20 - 30 °C
View Scheme
Multi-step reaction with 2 steps
1: 0 - 25 °C / Inert atmosphere; Industrial scale
2: hydrogenchloride / N,N-dimethyl acetamide; methanol / 15 °C / Reflux; Industrial scale
View Scheme
4-amino-2-trifluoromethylbenzonitrile
654-70-6

4-amino-2-trifluoromethylbenzonitrile

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: hexane; water / 36 h / 0 - 30 °C / Inert atmosphere
2: N,N-dimethyl acetamide / 1.5 h / 60 °C / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1.1: hexane; water / 36 h / 0 - 30 °C
2.1: N,N-dimethyl acetamide / 1.5 h / 60 °C
2.2: 20 - 30 °C
View Scheme
Multi-step reaction with 3 steps
1: sodium hydrogencarbonate / water; dichloromethane / 1.5 h / 0 - 20 °C
2: dmap / toluene / 16 h / 100 °C
3: hydrogenchloride; water / methanol / 2 h / 100 °C
View Scheme
p-benzyloxyaniline
6373-46-2

p-benzyloxyaniline

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: sodium hydrogencarbonate / 5 h / 150 °C / Inert atmosphere
2: dimethyl sulfoxide; Isopropyl acetate / 18 h / 25 - 82 °C / Inert atmosphere
3: boron tribromide / dichloromethane / 1.5 h / -78 °C / Inert atmosphere
View Scheme
methyl 2-(4-benzyloxyanilino)-2-methyl-propanoate
677703-47-8

methyl 2-(4-benzyloxyanilino)-2-methyl-propanoate

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: dimethyl sulfoxide; Isopropyl acetate / 18 h / 25 - 82 °C / Inert atmosphere
2: boron tribromide / dichloromethane / 1.5 h / -78 °C / Inert atmosphere
View Scheme
4-isothiocyanato 2-(trifluoromethyl)benzonitrile
143782-23-4

4-isothiocyanato 2-(trifluoromethyl)benzonitrile

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: dmap / toluene / 16 h / 100 °C
2: hydrogenchloride; water / methanol / 2 h / 100 °C
View Scheme
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

trifluoromethylsulfonic anhydride
358-23-6

trifluoromethylsulfonic anhydride

[4-[3-[4-cyano-3-(trifluoromethyl)phenyl]-5,5-dimethyl-4-oxo-2-thioxo-imidazolidin-1-yl]phenyl]trifluoromethanesulfonate

[4-[3-[4-cyano-3-(trifluoromethyl)phenyl]-5,5-dimethyl-4-oxo-2-thioxo-imidazolidin-1-yl]phenyl]trifluoromethanesulfonate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃; for 1h; Inert atmosphere;100%
tert-butyl 3-[2-[2-[2-(4-methylphenyl)sulfonyloxyethoxy]ethoxy]ethoxy]propanoate
217817-01-1

tert-butyl 3-[2-[2-[2-(4-methylphenyl)sulfonyloxyethoxy]ethoxy]ethoxy]propanoate

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

tert-butyl 3-(2-(2-(2-(4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)phenoxy)ethoxy)ethoxy)ethoxy)propanoate

tert-butyl 3-(2-(2-(2-(4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)phenoxy)ethoxy)ethoxy)ethoxy)propanoate

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 90℃; for 1h; Microwave irradiation;96%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

8-tosyloxy-3,6-dioxaoctanol
77544-68-4

8-tosyloxy-3,6-dioxaoctanol

4-[3-(4-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}phenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

4-[3-(4-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}phenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 20 - 80℃;91%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

epichlorohydrin
106-89-8

epichlorohydrin

4-(4,4-dimethyl-3-(4-(oxiran-2-ylmethoxy)phenyl)-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

4-(4,4-dimethyl-3-(4-(oxiran-2-ylmethoxy)phenyl)-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With potassium carbonate In acetonitrile at 80℃; for 16h; Inert atmosphere;58.8%
With potassium carbonate In acetonitrile at 80℃; for 16h;58.8%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

1,2-O-isopropylidene-D-glycerol
14347-78-5

1,2-O-isopropylidene-D-glycerol

(R)-4-(3-(4-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

(R)-4-(3-(4-((2,2-dimethyl-1,3-dioxolan-4-yl)methoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With tributylphosphine; 1,1'-azodicarbonyl-dipiperidine In toluene at 60 - 65℃; Industrial scale;53%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

1-bromoethanol
141072-57-3

1-bromoethanol

4-(3-(4-(2-hydroxyethoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl )-2-(trifluoromethyl)benzonitrile

4-(3-(4-(2-hydroxyethoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl )-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 12h; Inert atmosphere;36.3%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

2-bromoethanol
540-51-2

2-bromoethanol

4-(3-(4-(2-hydroxyethoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl )-2-(trifluoromethyl)benzonitrile

4-(3-(4-(2-hydroxyethoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl )-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 12h;36.3%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

tert-butyl (1-(hydroxymethyl)cyclopropyl)carbamate
107017-73-2

tert-butyl (1-(hydroxymethyl)cyclopropyl)carbamate

tert-butyl (1-((4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)phenoxy)methyl)cyclopropyl)carbamate

tert-butyl (1-((4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)phenoxy)methyl)cyclopropyl)carbamate

Conditions
ConditionsYield
With di-isopropyl azodicarboxylate; triphenylphosphine In dichloromethane for 2h; Inert atmosphere;35.2%
With di-isopropyl azodicarboxylate; triphenylphosphine In dichloromethane at 20 - 30℃; for 2h;35.2%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

tetraethylene glycol di(p-toluenesulfonate)
37860-51-8

tetraethylene glycol di(p-toluenesulfonate)

2-(2-(2-(2-(4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)phenoxy)ethoxy)ethoxy)ethoxy)ethyl 4-methylbenzenesulfonate

2-(2-(2-(2-(4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)phenoxy)ethoxy)ethoxy)ethoxy)ethyl 4-methylbenzenesulfonate

Conditions
ConditionsYield
With potassium carbonate In acetone at 110℃; for 1h; Microwave irradiation;32%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-2,5-dithioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-2,5-dithioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

Conditions
ConditionsYield
With Lawessons reagent In toluene for 15h; Heating / reflux;22%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

oxetan-3-yl 4-methylbenzenesulfonate
26272-83-3

oxetan-3-yl 4-methylbenzenesulfonate

4-(4,4-dimethyl-3-(4-((oxetan-3-yl)oxy)phenyl)-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

4-(4,4-dimethyl-3-(4-((oxetan-3-yl)oxy)phenyl)-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl acetamide at 80℃; for 12h; Inert atmosphere;17.7%
With potassium carbonate In N,N-dimethyl acetamide at 80℃; for 12h;17.7%
3,4-epoxytetrahydrofuran
285-69-8

3,4-epoxytetrahydrofuran

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

4-(3-(4-(((3R,4R/3S,4S)-4-hydroxytetrahydrofuran-3-yl)oxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

4-(3-(4-(((3R,4R/3S,4S)-4-hydroxytetrahydrofuran-3-yl)oxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl acetamide at 120℃; for 0.5h; Inert atmosphere;12.1%
With caesium carbonate In N,N-dimethyl acetamide at 120℃; for 0.5h;12.1%
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

chloroacetyl chloride
79-04-9

chloroacetyl chloride

chloroacetic acid 4-[3-(4-cyano-3-trifluoromethylphenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl]phenyl ester

chloroacetic acid 4-[3-(4-cyano-3-trifluoromethylphenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl]phenyl ester

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 4h;
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

(R)-4-(3-(4-(2,3-dihydroxypropoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

(R)-4-(3-(4-(2,3-dihydroxypropoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / toluene / 3 h / 50 °C / Inert atmosphere
2: acetic acid / water / 1 h / 70 °C / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / toluene / 3 h / 50 °C / Inert atmosphere
2: acetic acid / water / 1 h / 70 °C
View Scheme
4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
915086-32-7

4-[3-(4-hydroxyphenyl)-4,4-dimethyl-5-oxo-2-sulfanylideneimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

4-(3-(4-(2,3-dihydroxypropoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

4-(3-(4-(2,3-dihydroxypropoxy)phenyl)-4,4-dimethyl-5-oxo-2-thioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: potassium carbonate / acetonitrile / 16 h / 80 °C / Inert atmosphere
2: sulfuric acid / water; tetrahydrofuran / 4 h / Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1: potassium carbonate / acetonitrile / 16 h / 80 °C
2: sulfuric acid; water / tetrahydrofuran / 4 h / 20 - 30 °C
View Scheme

915086-32-7Relevant articles and documents

Systematic Investigation of the Permeability of Androgen Receptor PROTACs

Scott, Duncan E.,Rooney, Timothy P. C.,Bayle, Elliott D.,Mirza, Tashfina,Willems, Henriette M. G.,Clarke, Jonathan H.,Andrews, Stephen P.,Skidmore, John

supporting information, p. 1539 - 1547 (2020/06/25)

Bifunctional molecules known as PROTACs simultaneously bind an E3 ligase and a protein of interest to direct ubiquitination and clearance of that protein, and they have emerged in the past decade as an exciting new paradigm in drug discovery. In order to investigate the permeability and properties of these large molecules, we synthesized two panels of PROTAC molecules, constructed from a range of protein-target ligands, linkers, and E3 ligase ligands. The androgen receptor, which is a well-studied protein in the PROTAC field was used as a model system. The physicochemical properties and permeability of PROTACs are discussed.

PROTEIN-PROTEIN INTERACTION INDUCING TECHNOLOGY

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, (2017/10/17)

The present disclosure is based on the surprising and unexpected discovery that a ligand molecule with certain characteristics is able to bind to two protein molecules simultaneously and recruit them to form a transient or stable protein-protein interaction complex. The protein-protein interaction and other cross-domain interactions gained in this process contribute additional stabilization energy to the complex beyond the combination of the binary binding energies, and therefore, largely increase the binding potency of the ligand. Accordingly, the present disclosure provides a Protein-Protein Interaction Inducing Technology (PPIIT), which includes a method to design and identify the tripartite or bifunctional compounds and use such compounds to induce protein-protein interactions in various contexts. The present disclosure also provides a composition for the purpose of inducing protein-protein interactions.

IMIDAZOLINE DERIVATIVES, PREPARATION METHODS THEREOF, AND THEIR APPLICATIONS IN MEDICINE

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, (2015/09/22)

New imidazoline derivatives represented by formula (I): preparation methods thereof, pharmaceutical compositions comprising such derivatives, and applications of such derivatives in preparing androgen receptor antagonists and medicaments for treating diseases such as prostate cancer are described.

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