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19184-10-2

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19184-10-2 Usage

General Description

(Z)-1-Fluoro-1-propene is a chemical compound with the molecular formula C3H5F. It is a colorless, highly flammable gas with a sweet, ether-like odor. (Z)-1-Fluoro-1-propene is used as a building block in the production of various chemicals, such as pharmaceuticals and agrochemicals. It is also used in the synthesis of fluorinated organic compounds, which have applications in the fields of medicine, agriculture, and materials science. However, it is important to handle (Z)-1-Fluoro-1-propene with care, as it is toxic if inhaled and can cause skin and eye irritation. Additionally, it is a greenhouse gas and should be handled and disposed of responsibly to minimize its impact on the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 19184-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,8 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19184-10:
(7*1)+(6*9)+(5*1)+(4*8)+(3*4)+(2*1)+(1*0)=112
112 % 10 = 2
So 19184-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H5F/c1-2-3-4/h2-3H,1H3/b3-2-

19184-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1-fluoropropene

1.2 Other means of identification

Product number -
Other names 1c-fluoro-propene

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:19184-10-2 SDS

19184-10-2Downstream Products

19184-10-2Relevant articles and documents

KINETIC STUDY OF CHEMICALLY ACTIVATED FLUOROCYCLOPROPANE.

Dall'O,Heydtmann

, p. 24 - 30 (1987)

The photolysis of ketene at 313 nm was studied in the presence of fluoroethene and oxygen. The product formation was observed as a function of total pressure between 12 and 1080 mbar. Chemically activated fluorocyclopropane was formed by addition of singlet methylene to the double bond, and subsequent isomerization to the fluoropropenes as well as decomposition of these primary products to allene, propyne and HF was observed. The product yield was described by RRKM calculations; a stepladder deactivation model was used.

Isotopomer Distributions of Neutral Products from a Doubly Labeled Cation in the Gas Phase. Interconversion of 1-Fluoro-1-propyl Cation and 1-Fluoroisopropyl Cation on the C3H6F+ Potential Energy Surface

Shaler, Thomas A.,Morton, Thomas Hellman

, p. 6771 - 6779 (2007/10/02)

The title cations CH3CH2CHF+ (3) and CH3CHCH2F+ (4) are formed as transient intermediates in the gas phase.These are labile on the millisecond timescale as free ions but can be intercepted in ion-neutral complexes.When 3 is generated as free cation by reaction of CF3+ with propionaldehyde, it rearranges to (CH3)2CF+ (1), as shown by recovery of 2-fluoropropene as a neutral product from its deprotonation in an EBFlow experiment.The same neutral product is recovered when 1 is produced directly by reaction of acetone with CF3+ in the EBFlow.Neutral productsindicative of 3 and 4 (allyl fluoride and 1-fluoropropene) are recovered when these cations are formed in + PhO.> ion-neutral complexes by electron bombardment of CH3CDFCH2OPh (6).Analysis of the isotopic distribution in the recovered neutrals from EBFlow radiolysis of CH3CDF*CH2OPh (where the asterisked carbon is 13C-labeled) allows an assessment of the primary rearrangement pathways.The distribution of label is assayed by using 19F NMR.Rearrangement of the R+ moiety to form deuterated 1 occurs in about half of the complexes formed.In the remainder, methyl transfer (to form deuterated 3) is 2-3 times faster than fluoride transfer (to form deuterated 4).Scrambling of deuterium in the neutral products provides evidence that 3 and 4 interconvert within the ion-neutral complexes.

SYNTHESE D'ETHYLENIQUES MONOFLUORES

Baklouti, A.,Chaabouni, M. M.

, p. 181 - 190 (2007/10/02)

Monofluorinated ethylenic compounds have been prepared by action of potassium tertiobutylate either on 2-fluorotosylates or 2-fluorochlorides.In the case of 2-fluorochlorides the action, at higher temperature, of basic salt such as KF in ethylene glycol, may be used to prepare monofluorinated ethylenics compounds.

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