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Benzene, 1-chloro-4-[(1-fluoro-1,2-propadienyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

349146-83-4

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349146-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349146-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,1,4 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 349146-83:
(8*3)+(7*4)+(6*9)+(5*1)+(4*4)+(3*6)+(2*8)+(1*3)=164
164 % 10 = 4
So 349146-83-4 is a valid CAS Registry Number.

349146-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-4-(1-fluoropropa-1,2-dienylsulfanyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:349146-83-4 SDS

349146-83-4Downstream Products

349146-83-4Relevant academic research and scientific papers

Electrolytic partial fluorination of organic compounds. Part 60: Highly regioselective anodic fluorination of aryl propargyl sulfides

Riyadh, Sayed M,Ishii, Hideki,Fuchigami, Toshio

, p. 5877 - 5883 (2007/10/03)

Aryl propargyl sulfides were subjected to electrochemical fluorination in dimethoxyethane (DME) containing various fluoride supporting electrolytes using an undivided cell to provide the corresponding α-monofluorinated or α,α-difluorinated sulfides selectively as main products in good yields depending on the amount of electricity passed. The α,α-difluorinated sulfides were stable enough to be isolated while the α-monofluorinated ones were very unstable. The α-monofluorinated sulfides were readily converted into the corresponding stable α-monofluoroallenyl sulfides in good yields. Furthermore, synthetic utility of α-monofluoroallenyl sulfides was also investigated.

Electrolytic partial fluorination of organic compounds. Part 43: Highly regioselective anodic mono- and difluorination of propargyl sulfides and preparation of α-fluoroallenyl sulfides

Riyadh, Sayed M.,Ishii, Hideki,Fuchigami, Toshio

, p. 3009 - 3011 (2007/10/03)

The anodic fluorination of aryl propargyl sulfides in DME containing a fluoride supporting electrolyte using an undivided cell provided the corresponding α-mono- and α,α-difluorinated sulfides selectively, depending on the amount of electricity passed. The α-monofluorinated sulfides were readily converted into the corresponding α-fluoroallenyl sulfides in good to moderate yields.

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