DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:675-14-9
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Cas:675-14-9
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inquiryCyanuric fluoride Basic information Product Name: Cyanuric fluoride Synonyms: 2,4,6-TRIFLUORO-1,3,5-TRIAZINE;CYANURIC FLUORIDE;1,3,5-triazine,2,4,6-trifluoro-;2,4,6-trifluoro-s-triazin;2
Cas:675-14-9
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Cas:675-14-9
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inquiryProduct name: Cyanuric Fluoride; 2,4,6-Trifluoro-1,3,5-triazine CAS No.: 675-14-9 Molecular formula: C3F3N3 Molecular weight: 174.12 Structural form
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J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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Cas:675-14-9
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inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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Conditions | Yield |
---|---|
With sulfolane; sodium fluoride at 150℃; Reagent/catalyst; Large scale; | 97% |
With tetrabutyl ammonium fluoride In dimethyl sulfoxide at 60℃; for 6h; Temperature; Solvent; | 95% |
With 1-methyl-pyrrolidin-2-one; hydrogen fluoride; triethylamine at 20 - 25℃; for 0.5h; | 90% |
1,3,5-trichloro-2,4,6-triazine
antimony(III) fluoride
trifluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
With antimony(III) chloride; chlorine 160-180°C, 10 mol SbF3, 1 mol SbCl3, 3 mol Cl2; | 91% |
With antimony(III) chloride; chlorine 160-180°C, 10 mol SbF3, 1 mol SbCl3, 3 mol Cl2; | 91% |
With chlorine at 100°C, exclusion of H2O; destillation; | 71.4% |
4-N,N-dichloroamino-2,3,5,6-tetrafluoropyridine
A
trifluoro-[1,3,5]triazine
B
4-chloro-2,3,5,6-tetrafluoropyridine
C
Pentafluoropyridine
D
trichlorofluoromethane
E
2-chloro-3,3-difluoro-acrylonitrile
F
tetrafluoropyrazine
Conditions | Yield |
---|---|
at 550℃; under 2 Torr; Mechanism; vacuum pyrolysis, other fluoropyridine compounds; | A n/a B 75% C n/a D n/a E n/a F n/a |
1,2,3-trifluoro-4,5,6-triazine
perfluoro-4,6-di-isopropyl-1,2,3-triazine
A
trifluoro-[1,3,5]triazine
B
perfluoro-2,4-di-isopropylpyridine
C
perfluoro-2,4,6,8-tetraisopropyl-1,5-diazatricyclo<4.2.0.02,5>octa-3,7-diene
Conditions | Yield |
---|---|
In 1,1,2-Trichloro-1,2,2-trifluoroethane for 24h; Irradiation; | A 0.01 g B 53% C 11% |
In 1,1,2-Trichloro-1,2,2-trifluoroethane for 24h; Irradiation; | A 0.01 g B 4% C 11 g |
In 1,1,2-Trichloro-1,2,2-trifluoroethane for 24h; Mechanism; Irradiation; | A 0.01 g B 0.17 g C 0.03 g |
1,3,5-trichloro-2,4,6-triazine
A
trifluoro-[1,3,5]triazine
B
2-chloro-4,6-difluoro-[1,3,5]triazine
C
2,4-dichloro-6-fluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
With potassium fluoride at 300℃; for 2h; Product distribution; C3Cl3N3/KF = 16 x 10 E-2, other temperatures, other times, other molar ratios; | A n/a B n/a C 48% |
With cesium fluoride; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate at 80℃; |
1,3,5-trichloro-2,4,6-triazine
sulfur tetrafluoride
trifluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
in 1:6 molar ratio, at 250°C, in autoclave; | 40% |
nitrogen trifluoride
cyanogen chloride
A
trifluoro-[1,3,5]triazine
B
cis-hexafluoroazomethane
C
Perfluoro-2-azapropen
Conditions | Yield |
---|---|
In not given at 500°C, in Ni-tube, in excess of NF3; | A 40% B 30% C 30% |
trifluoro-1,2,4-triazine
A
trifluoro-[1,3,5]triazine
B
Perfluoro-2-azapropen
Conditions | Yield |
---|---|
at 500℃; for 42h; | A 32% B 12% C n/a |
1,3,5-trichloro-2,4,6-triazine
A
trifluoro-[1,3,5]triazine
B
2-chloro-4,6-difluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
With antimonypentachloride; antimony(III) fluoride | |
With antimonypentachloride; antimony(III) fluoride melting, heating, 1 h distn.; fractionated distn.; | |
With SbF3; SbCl5 melting, heating, 1 h distn.; fractionated distn.; |
1,3,5-trichloro-2,4,6-triazine
antimony(III) fluoride
antimony(III) chloride
chlorine
trifluoro-[1,3,5]triazine
1,3,5-trichloro-2,4,6-triazine
hydrogen fluoride
A
trifluoro-[1,3,5]triazine
B
2-chloro-4,6-difluoro-[1,3,5]triazine
C
2,4-dichloro-6-fluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
auch unter Zusatz von Sb2O3 oder SbCl5; | |
With SbCl5 |
1,3,5-trichloro-2,4,6-triazine
A
trifluoro-[1,3,5]triazine
B
2-chloro-4,6-difluoro-[1,3,5]triazine
C
2,4-dichloro-6-fluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
auch unter Zusatz von Sb2O3 oder SbCl5; | |
auch unter Zusatz von Sb2O3 oder SbCl5; |
1,3,5-trichloro-2,4,6-triazine
A
trifluoro-[1,3,5]triazine
B
2-chloro-4,6-difluoro-[1,3,5]triazine
C
2,4-dichloro-6-fluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
auch unter Zusatz von Sb2O3 oder SbCl5; | |
auch unter Zusatz von Sb2O3 oder SbCl5; |
1,3,5-trichloro-2,4,6-triazine
A
trifluoro-[1,3,5]triazine
B
2-chloro-4,6-difluoro-[1,3,5]triazine
C
2,4-dichloro-6-fluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
auch unter Zusatz von Sb2O3 oder SbCl5; | |
auch unter Zusatz von Sb2O3 oder SbCl5; |
Trifluoromethylsulfenyl chloride
1,3,5-Trichlor-2,2,4,4,6,6-hexafluor-1,3,5-triazinan
A
trifluoro-[1,3,5]triazine
B
Bis(trifluoromethyl)disulfid
C
trifluoromethanesulfinyl fluoride
Conditions | Yield |
---|---|
byproducts: Cl2; at 20°C (1 h); | |
byproducts: Cl2; at 20°C (1 h); |
cis-hexafluoroazomethane
A
trifluoro-[1,3,5]triazine
B
carbon tetrafluoride
C
N,N-Bis(trifluoromethyl)amine
D
Perfluoro-2-azapropen
E
tetrakis(trifluoromethyl)hydrazine
Conditions | Yield |
---|---|
heating in autoclave at 483°C; further product; | |
heating in autoclave at 483°C; further product; |
Conditions | Yield |
---|---|
at ambient temp. quick polimn.; | |
room temp., polymerisation; | |
at ambient temp. quick polimn.; |
2,2,2-trifluoro-1-oxoethanesulphenylchloride
1,3,5-Trichlor-2,2,4,4,6,6-hexafluor-1,3,5-triazinan
A
trifluoro-[1,3,5]triazine
B
2,2,2-trifluoro-1-oxoethanesulfenyl fluoride
Conditions | Yield |
---|---|
byproducts: Cl2; | |
byproducts: Cl2; |
1,3,5-trichloro-2,4,6-triazine
A
trifluoro-[1,3,5]triazine
B
2-chloro-4,6-difluoro-[1,3,5]triazine
C
2,4-dichloro-6-fluoro-[1,3,5]triazine
D
Hexafluormethandiamin
E
cycloperfluoro dimethylenediamine
Conditions | Yield |
---|---|
With fluorine 125°C, under N2; |
Conditions | Yield |
---|---|
other products, in N2, at 125°C; |
2-chloro-4,6-difluoro-[1,3,5]triazine
2,4-dichloro-6-fluoro-[1,3,5]triazine
1,3,5-trichloro-2,4,6-triazine
trifluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
With Sb2O3; KHF2 In benzene | |
With KF | |
With KHF2 |
cyanuric bromide
trifluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
With ZnF2 | |
With KF; Sb2O3 |
dichloromethylene-trifluoromethylmercaptoamine
A
trifluoro-[1,3,5]triazine
C
bis(trifluoromethylmercapto)-trifluoromethylamine
Conditions | Yield |
---|---|
byproducts: AgCl; 130°C; 21 h;; detected by IR and Mass spectr.; | |
byproducts: AgCl; 130°C; 21 h;; detected by IR and Mass spectr.; |
manganese(III) fluoride
cyanogen chloride
A
trifluoro-[1,3,5]triazine
B
carbon tetrafluoride
C
chlorotrifluoromethane
D
pentafluoro chloro azomethane
Conditions | Yield |
---|---|
byproducts: Cl2; at 160-190°C; |
nitrogen trifluoride
cyanogen chloride
A
trifluoro-[1,3,5]triazine
B
carbon tetrafluoride
C
cis-hexafluoroazomethane
D
trichlorofluoromethane
E
Perfluoro-2-azapropen
Conditions | Yield |
---|---|
With chlorine In not given at 450-500°C, in Ni-tube, in excess of NF3; |
Conditions | Yield |
---|---|
In not given ClCN/NF3 = 1:1; |
trifluoro-[1,3,5]triazine
tris(dimethylamino)sulfonium trimethylsilyldifluoride
Conditions | Yield |
---|---|
In acetonitrile at -196 - -40℃; for 0.75h; | 100% |
trifluoro-[1,3,5]triazine
(2R)-2-({formyl[(phenylmethyl)oxy]amino}methyl)hexanoic acid
(2R)-2-({formyl[(phenylmethyl)oxy]amino}methyl)hexanoyl fluoride
Conditions | Yield |
---|---|
With pyridine | 100% |
trifluoro-[1,3,5]triazine
6-chloro-2-(ethylamino)pyridine-3-carboxylic acid
6-chloro-2-(ethylamino)pyridine-3-carbonyl fluoride
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 3h; | 99% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide Inert atmosphere; | 98% |
trifluoro-[1,3,5]triazine
trifluoroethylamine
2-fluoro-4,6-bis<(2,2,2-trifluoroethyl)amino>-1,3,5-triazine
Conditions | Yield |
---|---|
97% |
trifluoro-[1,3,5]triazine
2-fluoro-4,6-bis<(2,2,2-trifluoroethyl)amino>-1,3,5-triazine
Conditions | Yield |
---|---|
97% |
trifluoro-[1,3,5]triazine
Conditions | Yield |
---|---|
With pyridine In dichloromethane | 96% |
trifluoro-[1,3,5]triazine
3-phenyl-4-(trifluoromethyl)isoxazole-5-carboxylic acid
3-phenyl-4-(trifluoromethyl)isoxazole-5-carbonyl fluoride
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 20℃; | 96% |
Conditions | Yield |
---|---|
In tetrahydrofuran hydrolysis at 0°C; | 94% |
In water hydrolysis at 0°C; | >99 |
trifluoro-[1,3,5]triazine
Propargylamine
N2,N4,N6-tri(prop-2-yn-1-yl)-1,3,5-triazine-2,4,6-triamine
Conditions | Yield |
---|---|
In toluene for 20h; Heating; | 93% |
In toluene Reflux; | 83% |
trifluoro-[1,3,5]triazine
trifluoroethylamine
2,4,6-tris<(2,2,2-trifluoroethyl)amino>-1,3,5-triazine
Conditions | Yield |
---|---|
With cesium fluoride In N,N-dimethyl-formamide at 40℃; for 72h; | 91% |
With cesium fluoride In N,N-dimethyl-formamide |
trifluoro-[1,3,5]triazine
N-tert-butoxycarbonyl-3-(2-naphthyl)-L-alanine
Conditions | Yield |
---|---|
With pyridine In dichloromethane at -15℃; for 1h; | 91% |
trifluoro-[1,3,5]triazine
2-[N-(tert-butoxycarbonyl)-N-(2,2,2-trifluoroethyl)aminomethyl]-4-methoxydihydrocinnamic acid
(R)-4-(phenylmethyl)-2-oxazolidinone
Conditions | Yield |
---|---|
With pyridine; n-butyllithium; ammonium chloride In tetrahydrofuran; dichloromethane | 91% |
trifluoro-[1,3,5]triazine
ferrocenylamidoundecanoic acid
ferrocenylamidoundecanoic acid fluoride
Conditions | Yield |
---|---|
With pyridine In dichloromethane (Ar, Schlenk technique); addn. of cyanuric fluoride to suspn. of ferrocene deriv. and pyridine in dry CH2Cl2, stirring for 2 h; addn. of ice cold water, filtration, separating organic layer, washing with cold water, drying over MgSO4, filtration, evapn., elem. anal.; | 91% |
polytetrafluoroethylene
trifluoro-[1,3,5]triazine
tris(perfluoroethyl)-s-triazine
Conditions | Yield |
---|---|
at 140℃; Large scale; | 91% |
trifluoro-[1,3,5]triazine
2-[N-(tert-butoxycarbonyl)-N-(4-trifluoromethylbenzyl)aminomethyl]-4-methoxydihydrocinnamic acid
(R)-4-(phenylmethyl)-2-oxazolidinone
Conditions | Yield |
---|---|
With pyridine; n-butyllithium; ammonium chloride In tetrahydrofuran; dichloromethane | 90% |
With pyridine; n-butyllithium; ammonium chloride In tetrahydrofuran; dichloromethane | 90% |
trifluoro-[1,3,5]triazine
K{Mn(CO)5}
Conditions | Yield |
---|---|
In not given -18°C; sublimed in vacuo (50°C/0.01 Torr), recrystd. from dry hexane; | 90% |
trifluoro-[1,3,5]triazine
perfluoropropylene
perfluoro-2,4,6-triisopropyl-s-triazine
Conditions | Yield |
---|---|
at 140℃; Reagent/catalyst; Temperature; Large scale; | 89% |
trifluoro-[1,3,5]triazine
glycine ethyl ester hydrochloride
2-[(4-[1-(tert-butoxycarbonyl)-4-piperidyl]-2-{2-[1-(tert-butoxycarbonyl)-4-piperidyl]ethyl}butanoyl)amino]acetic acid
Conditions | Yield |
---|---|
With pyridine; hydrogenchloride; lithium hydroxide monohydrate; N-ethyl-N,N-diisopropylamine In tetrahydrofuran; dichloromethane; water | 88% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide | 87% |
In N,N-dimethyl-formamide |
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 20℃; for 2.5h; | 87% |
trifluoro-[1,3,5]triazine
boron trifluoride diethyl etherate
2,3-Dihydro-1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene
2-(4,6-difluoro-1,3,5-triazin-2-yl)-1,3-diisopropyl-4,5-dimethylimidazolium tetrafluoroborate
Conditions | Yield |
---|---|
In diethyl ether (Ar); imidazolylidene deriv. added to Et2O soln. of cyanuric trifluorideat -70°C; stirred for 12 h at room temp.; BF3*OEt2 added dropwis e; stirred for 4 h at room temp.; ppt. isolated; washed with Et2O; vac. dried; recrystd. from MeCN/Et2O; elem. anal.; | 86% |
trifluoro-[1,3,5]triazine
(R)-4-(phenylmethyl)-2-oxazolidinone
Conditions | Yield |
---|---|
With pyridine; n-butyllithium In tetrahydrofuran; dichloromethane | 85% |
Conditions | Yield |
---|---|
With pyridine In acetonitrile | 85% |
trifluoro-[1,3,5]triazine
2,3-Dihydro-1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene
2-(4,6-difluoro-1,3,5-triazin-2-yl)-1,3-diisopropyl-4,5-dimethylimidazolium tetrafluoroborate
Conditions | Yield |
---|---|
Stage #1: trifluoro-[1,3,5]triazine; 2,3-Dihydro-1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene In diethyl ether at -70 - 20℃; Inert atmosphere; Stage #2: With boron trifluoride diethyl etherate at 20℃; Inert atmosphere; | 85% |
trifluoro-[1,3,5]triazine
(Sp)-2-formylferrocene-1-carboxylic acid
(Sp)-2-formylferrocenoyl fluoride
Conditions | Yield |
---|---|
With pyridine In dichloromethane pyridine (1.650 ml) and cyanuric fluoride (3.605 ml) added to CH2Cl2 soln. of Fc(CHO)CO2H (10 mmol) at 0°C under Ar, after few min cooling bath removed, mixt. stirred at room temp. for 90 min; crushed ice added, suspn. filtered, organic phase sepd., washed with cold H2O, dried over Na2SO4, filtered, solidified for few min, crystals collected, dried in vac. exicator over P2O5 overnight at room temp.; elem. anal.; | 85% |
trifluoro-[1,3,5]triazine
A
fluorocarbonyl ruthenocene
B
[Ru(η5-C5H5)(η5-C5H4CO)]2O
Conditions | Yield |
---|---|
With pyridine In dichloromethane under N2 or Ar; suspn. of Ru complex and pyridine in CH2Cl2 cooled to 0°C; N3C3F3 added; stirred at 0°C for 2 h; poured into ice-cold H2O; filtered; org. layer collected; concd. in vac.; purified by column chromy. (silica gel, ethyl acetate-hexane 1:5); elem. anal.; | A 82% B 2% |
Conditions | Yield |
---|---|
Stage #1: trifluoro-[1,3,5]triazine; sulfanilamide In acetone at 0℃; for 0.5h; Stage #2: With sodium hydroxide In water; acetone at 20℃; for 1.33333h; | 82% |
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