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Benzene, 1-(2-fluoro-2-propenyl)-4-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128259-86-9

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128259-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128259-86-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,5 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128259-86:
(8*1)+(7*2)+(6*8)+(5*2)+(4*5)+(3*9)+(2*8)+(1*6)=149
149 % 10 = 9
So 128259-86-9 is a valid CAS Registry Number.

128259-86-9SDS

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 1-(2-fluoroprop-2-enyl)-4-methoxybenzene

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:128259-86-9 SDS

128259-86-9Relevant academic research and scientific papers

Halofluorination of Alkenes Using Dilute Hydrofluoric Acid

Kuroboshi, Manabu,Hiyama, Tamejiro

, p. 1799 - 1806 (2007/10/03)

Iodofluorination of alkenes was achieved with N-iodosuccinimide, potassium hydrogendifluoride, and 1 M hydrofluoric acid using tetrabutylammonium fluoride as a phase-transfer catalyst.The active fluorinating reagent was shown to be tetrabutylammonium dihy

Halofluorination of Alkenes Using Tetrabutylammonium Dihydrogentrifluoride

Kuroboshi, Manabu,Hiyama, Tamejiro

, p. 1215 - 1218 (2007/10/02)

Regio-, stereo-, and chemoselective halofluorination of alkenes is achieved using N-haloamides and tetrabutylammonium dihydrogentrifluoride, and the resulting F-I adducts were successfully converted into fluoroalkenes under dehydroiodation with 1,8-diazab

PHARMACEUTICALLY ACTIVE 3-HETEROARYL-2-FLUORO-1-OLEFINS

-

, (2008/06/13)

This invention relates to novel 3-heteroaryl-2-fluoro-l-olefins and their pharmacological use as dopamine beta-hydroxylase DBH inhibitors in the treatment of DBH mediated conditions such as hypertension.

Novel process for the synthesis of 2-fluoro-1-olefins

-

, (2008/06/13)

A process for preparing 2-fluoro-1-olefins or terminal bis-beta-fluoro-olefins which comprises reacting an appropriate allyl or alpha-olefinated starting material with phenylselenyl chloride and silver fluoride, and then reacting the intermediate phenylselenyl fluoride compound with ozone, and further reacting the resulting phenylselenoxide compound with an appropriate amine, to yield the desired fluorinated compounds.

A new synthesis of 2-fluoro-1-olefins

McCarthy, James R.,Matthews, Donald P.,Barney, Charlotte L.

, p. 973 - 976 (2007/10/02)

The first examples of the addition of PhSeF to olefins to yield β-fluoro phenylselenides (2) are reported. β-Fluoro phenylselenides (2) obtained from terminal olefins were converted to the title vinyl fluorides 3 on treatment with ozone, whereas, 2 obtain

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