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3,5-Bis(trifluoromethyl)phenylacetylene

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3,5-Bis(trifluoromethyl)phenylacetylene manufacturers

3,5-Bis(trifluoromethyl)phenylacetylene Basic information
Uses
Product Name:3,5-Bis(trifluoromethyl)phenylacetylene
Synonyms:3',5'-BIS-TRIFLUOROMETHYLPHENYL ACETYLENE;3,5-BIS(TRIFLUOROMETHYL)-1-ETHYNYLBENZENE;SALOR-INT L308668-1EA;1-ETHYNYL-3,5-BIS(TRIFLUOROMETHYL)BENZE&;3,5-Bis(trifluoromethyl)phenylacetylene 99+%;Benzene, 1-ethynyl-3,5-bis(trifluoroMethyl;1,3-Bis(trifluoromethyl)-5-ethynylbenzene;1-Ethynyl-3,5-bis(trifluoroMethyl)benzene 97%
CAS:88444-81-9
MF:C10H4F6
MW:238.13
EINECS:
Product Categories:Miscellaneous;Alkynyl;Halogenated Hydrocarbons;Organic Building Blocks
Mol File:88444-81-9.mol
3,5-Bis(trifluoromethyl)phenylacetylene Structure
3,5-Bis(trifluoromethyl)phenylacetylene Chemical Properties
Boiling point 147-148 °C (lit.)
density 1.346 g/mL at 25 °C (lit.)
refractive index n20/D 1.4230(lit.)
Fp 112 °F
storage temp. 2-8°C
form clear liquid
color Colorless to Light yellow to Light orange
InChIInChI=1S/C10H4F6/c1-2-6-3-7(9(11,12)13)5-8(4-6)10(14,15)16/h1,3-5H
InChIKeyMAHIBRPXUPUAIF-UHFFFAOYSA-N
SMILESC1(C#C)=CC(C(F)(F)F)=CC(C(F)(F)F)=C1
CAS DataBase Reference88444-81-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 10-36/37/38
Safety Statements 16-26-36
RIDADR UN 1993 3/PG 3
WGK Germany 3
Hazard Note Irritant
HazardClass 3
HS Code 29039990
Storage Class3 - Flammable liquids
Hazard ClassificationsEye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
3,5-Bis(trifluoromethyl)phenylacetylene Usage And Synthesis
Uses3,5-Bis(trifluoromethyl)phenylacetylene is a useful research chemical.
Chemical PropertiesYellow liquid
Synthesis
(3,5-BIS(TRIFLUOROMETHYL)PHENYLETHYNYL)&

618092-28-7

3,5-BIS(TRIFLUOROMETHYL)PHENYLACETYLENE

88444-81-9

General procedure for the synthesis of 3,5-bis(trifluoromethyl)phenylethynyltrimethylsilane from (3,5-bis(trifluoromethyl)phenylethynyl)trimethylsilane: To a mixed solution of 2-[3,5-bis(trifluoromethyl)phenyl]ethynyltrimethylsilane (83.1g, 267.7mmol) in methanol (70mL) and chloroform (70mL) was added potassium carbonate (7.4g, 53.5 mmol), followed by stirring the reaction mixture at room temperature overnight. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. Water was added to the residue and extracted with ether. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. After filtration to remove the desiccant, the filtrate was concentrated under reduced pressure to give the crude product. The crude product was further purified by reduced pressure distillation (82 °C, 100 mbar) to afford 3,5-bis(trifluoromethyl)phenylacetylene (48.7 g, 76% yield) as a colorless oil. The structure of the product was confirmed by 1H NMR (CDCl3): δ 7.92 (2H, s), 7.84 (1H, s), 3.26 (1H, s).

References[1] Dalton Transactions, 2012, vol. 41, # 3, p. 839 - 849
[2] Patent: US2018/290986, 2018, A1. Location in patent: Paragraph 0230; 0231
[3] Journal of Organic Chemistry, 1993, vol. 58, # 24, p. 6614 - 6619
[4] Chemical Communications, 2008, # 19, p. 2203 - 2205
[5] Journal of Materials Chemistry C, 2017, vol. 5, # 31, p. 7977 - 7984
3,5-Bis(trifluoromethyl)phenylacetylene Preparation Products And Raw materials
Raw materials(3,5-Bis(trifluoromethyl)phenylethynyl)&-->Chloroform-->Methanol-->Potassium carbonate
Tag:3,5-Bis(trifluoromethyl)phenylacetylene(88444-81-9) Related Product Information
4'-Trifluoromethylphenyl acetylene Phenylacetylene 3,5-Bis(trifluoromethyl)phenylacetylene 2,5-bis(trifluoromethyl)phenylacetylene FLUPROPADINE (3-[3,5-Di(trifluoromethyl)phenyl]prop-2-ynyl)(triethyl)ammonium bromide 3,5-Bis(trifluoromethyl)diphenylacetylene Bis[3,5-bis(trifluoromethyl)phenyl]acetylene 3-[3,5-Di(trifluoromethyl)phenyl]prop-2-ynyl N-(1,2,2-trichlorovinyl)carbamate 1-(3,5-Bis(trifluoromethyl)phenyl)-3-hydroxy-3-methyl-1-butyne 4-[3,5-Bis(trifluoromethyl)phenyl]-3-butyn-2-ol (3,5-Bis(trifluoromethyl)phenylethynyl)& 3-[3,5-Di(trifluoromethyl)phenyl]prop-2-ynyl 2-chloroacetate 1-(3-Bromoprop-1-ynyl)-3,5-di(trifluoromethyl)benzene N-(3-[3,5-Bis(trifluoromethyl)phenyl]-1,1-dimethylprop-2-ynyl)-2-chloroacetamide 3-[3,5-Bis(trifluoromethyl)phenyl]prop-2-yn-1-ol