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Ethanone, 2,2-difluoro-2-(methylthio)-1-phenyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192862-16-1

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192862-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192862-16-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,8,6 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 192862-16:
(8*1)+(7*9)+(6*2)+(5*8)+(4*6)+(3*2)+(2*1)+(1*6)=161
161 % 10 = 1
So 192862-16-1 is a valid CAS Registry Number.

192862-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-difluoro-2-methylsulfanyl-1-phenylethanone

1.2 Other means of identification

Product number -
Other names 2,2-difluoro-2-(methylthio)acetophenone

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:192862-16-1 SDS

192862-16-1Relevant articles and documents

Process for the production of fluorinated organic compounds and fluorinating agents

-

, (2008/06/13)

A process for the production of a fluorinated organic compound, characterized by fluorinating an organic compound having a hydrogen atoms using IF5; and a novel fluorination process for fluorinating an organic compound having a hydrogen atoms by using a fluorinating agent containing IF5 and at least one member selected from the group consisting of acids, bases, salts and additives.

Fluorination of sulfides using IF5-Et3N-3HF

Ayuba, Shinichi,Yoneda, Norihiko,Fukuhara, Tsuyoshi,Hara, Shoji

, p. 1597 - 1603 (2007/10/03)

Mono- and difluorinations of sulfides were achieved using a novel fluorinating reagent, IF5-Et3N-3HF. The reagent is applicable for substrates having various electron-withdrawing groups, such as an ester, amide, ketone, ni

New antifungal 1,2,4-triazoles with difluoro(substituted sulfonyl)methyl moiety

Eto,Kaneko,Takeda,Tokizawa,Sato,Yoshida,Namiki,Ogawa,Maebashi,Ishida,Matsumoto,Asaoka

, p. 173 - 182 (2007/10/03)

New 1,2,4-triazoles (2) having a difluoro(substituted sulfonyl)methyl moiety were designed and synthesized via α,α-difluoro-α-(substituted thio)acetophenones (3). Compounds (2) showed potent antifungal activities against C. albicans, C. krusei, A. flavus

α, α-gem-difluorination of α-(alkylthio)acetophenone derivatives with N-Fluoropyridinium salts

Takeda, Sunao,Kaneko, Yasushi,Eto, Hiromichi,Tokizawa, Minoru,Sato, Susumu,Yoshida, Kouiti,Namiki, Setsuo,Ogawa, Masaki

, p. 1097 - 1100 (2007/10/03)

The α, α-gem-difluorination of 2',4'-difluoro- α(methylthio)acetophenone (1a) with N-fluoropyridinium salts gave 2',4',α-tetrafluoro-α-(methylthio)acetophenone (3a). This reaction was accelerated by the addition of zinc chloride, zinc bromide or anhydrous iron(III) chloride, and higher yields than the reaction without additives were obtained. The gem- difluorination reaction using FP-T300 in the presence of zinc bromide was applicable to other α-(alkylthio)acetophenone derivatives (1).

Triazole derivative and pharmaceutical comprising the same as an effective ingredient

-

, (2008/06/13)

Described is a triazole derivative represented by the formula (1) or salt thereof, preparation process thereof, preparation intermediates represented by the formulas (2) and (3), and a pharmaceutical comprising the compound represented by the formula (1)

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