Cas 1214756-34-9,2-phenyl-1-(trifluoromethyl)-1H-benzo[b]thiophen-1-ium trifluoromethanesulfonate

1214756-34-9

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Basic information

Product Name: 2-phenyl-1-(trifluoromethyl)-1H-benzo[b]thiophen-1-ium trifluoromethanesulfonate
Synonyms: 2-phenyl-1-(trifluoromethyl)-1H-benzo[b]thiophen-1-ium trifluoromethanesulfonate
CAS NO:1214756-34-9
Molecular Formula:
Molecular Weight: 428.376
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-phenyl-1-(trifluoromethyl)-1H-benzo[b]thiophen-1-ium trifluoromethanesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: 2-phenyl-1-(trifluoromethyl)-1H-benzo[b]thiophen-1-ium trifluoromethanesulfonate(1214756-34-9)
EPA Substance Registry System: 2-phenyl-1-(trifluoromethyl)-1H-benzo[b]thiophen-1-ium trifluoromethanesulfonate(1214756-34-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1214756-34-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1214756-34-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,7,5 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1214756-34:
(9*1)+(8*2)+(7*1)+(6*4)+(5*7)+(4*5)+(3*6)+(2*3)+(1*4)=139
139 % 10 = 9
So 1214756-34-9 is a valid CAS Registry Number.

1214756-34-9Upstream product

1214756-34-9Downstream Products

1214756-34-9Relevant academic research and scientific papers

Silver-Mediated Trifluoromethylthiolation-Iodination of Arynes

Zeng, Yuwen,Hu, Jinbo

, p. 856 - 859 (2016)

(Chemical Equation Presented). A one-pot trifluoromethylthiolation-iodination of arynes with trifluoromethylthiosilver (AgSCF3) and 1-iodophenylacetylene is described. This protocol allows rapid construction of o-trifluoromethylthiolated arene building blocks in moderate yields. These products were found to be excellent precursors for Yagupolskii-Umemoto-type electrophilic trifluoromethylation reagents.

TRIFLUOROMETHYLTHIOPHENIUM DERIVATIVE SALT, METHOD FOR PRODUCING THE SAME, AND METHOD FOR PRODUCING TRIFLUOROMETHYL-CONTAINING COMPOUNDS USING THE SAME

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Page/Page column 18, (2012/06/01)

A trifluoromethylthiophenium derivative salt useful as synthetic intermediates for pharmaceuticals and agrochemicals, a method for producing the same, and a method for producing trifluoromethyl-containing compounds using the same are provided. An S-(trifl

Efficient access to extended yagupolskii-umemoto-type reagents: Triflic acid catalyzed intramolecular cyclization of ortho- ethynylaryltrifluoromethylsulfanes

Matsnev, Andrej,Noritake, Shun,Nomura, Yoshinori,Tokunaga, Etsuko,Nakamura, Shuichi,Shibata, Norio

supporting information; experimental part, p. 572 - 576 (2010/04/05)

(Figure Presented) King of the ring: S-(trifluoromethyl)benzo[b]thiophenium salts 1, as analogues of Yagupolskii-Umemoto type reagents, were synthesized by novel triflic acid catalyzed intramolecular cyclization of ortho- ethynylaryltrifluoromethylsulfane

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