Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1691-13-0

Post Buying Request

1691-13-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1691-13-0 Usage

General Description

1,2-Difluoroethylene, also known as 1,2-difluoroethene, is a colorless, highly flammable gas that is used in the production of specialty chemicals and polymers. It has a distinct sweet odor and is commonly utilized as a monomer in the synthesis of poly(vinylidene fluoride), a high-performance thermoplastic with excellent resistance to chemicals, heat, and weathering. 1,2-Difluoroethylene is also employed as a refrigerant and in the manufacturing of fluorinated compounds for various applications, including pharmaceuticals, agrochemicals, and electronics. However, it is important to handle and store 1,2-difluoroethylene with caution, as exposure to this compound can cause irritation to the respiratory tract and other adverse health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1691-13-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1691-13:
(6*1)+(5*6)+(4*9)+(3*1)+(2*1)+(1*3)=80
80 % 10 = 0
So 1691-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C2H2F2/c3-1-2-4/h1-2H

1691-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-DIFLUOROETHYLENE

1.2 Other means of identification

Product number -
Other names 1,2-fluoroethene

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:1691-13-0 SDS

1691-13-0Relevant articles and documents

Anomalous elimination of HCl from 2-chloro-1,1-difluoroethane. Likely involvement of a 1,2-FCl interchange mechanism

Dolbier Jr., William R.,Romelaer, Raphaele,Baker, J.Marshall

, p. 8075 - 8077 (2002)

A novel 1,2-FCl interchange mechanism is proposed to be involved in the unexpected thermal conversion of CH2ClCHF2 to 1,2-difluoroethylene.

Vibrationally excited populations from IR-multiphoton absorption. II. Infrared fluorescence measurements

Zellweger, Jean-Michel,Brown, Trevor C.,Barker, John R.

, p. 6261 - 6267 (1985)

Infrared emission spectra were obtained for 1,1,2-trifluoroethane (TFE) excited by infrared multiphoton absorption (1079.85 cm-1).The emission features show that the HF reaction product is formed in vibrational states up to about v = 3.Furthermore, emission attributed to F-CC-H was observed near 3320 cm-1, indicating that the difluoroethylene primary products of TFE decomposition undergo secondary photolysis; since the difluoroethylene products at room temperature do not absorb laser light, they must be formed vibrationally excited.The emission from the C-H stretch modes of TFE was readily identified near 2980 cm-1 and the emission intensity was obtained as a function of laser fluence.These data are in excellent agreement with predictions based on the theoretical expression for fluorescence intensity and the reconstructed populations determined by the Master Equation calculations described in the preceding paper.These results provide additional support for the accuracy of the reconstructed population distributions and for the theory relating infrared fluorescence intensity to total vibrational energy in polyatomic molecules.

Gas-phase kinetics of the self reactions of the radicals CH2F and CHF2

Beiderhase, Thomas,Hack, Walter,Hoyermann, Karlheinz,Olzmann, Matthias

, p. 625 - 641 (2000)

Fluorinated hydrocarbon radical-radical reactions in the gas phase have been studied at low pressure (0.5 ≤ p/mbar ≤ 2) and low temperature (253 ≤ T/K ≤ 333) using the discharge flow reactor molecular beam sampling mass spectrometry (MS) technique. Stable

METHOD FOR PRODUCING 1-CHLORO-1,2-DIFLUOROETHYLENE

-

Paragraph 0115, (2019/06/17)

The present invention provides a method for efficiently producing 1-chloro-1,2-difluoroethylene at low cost. Specifically, the present invention provides a method for producing 1-chloro-1,2-difluoroethylene, including the step of dehydrohalogenating chlorofluoroethane represented by formula (1) CFClX1—CHFX2 wherein X1 and X2 are different from each other and represent H, F, or Cl; and either X1 or X2 is H.

Copper-Catalyzed Difluoromethylation of Aryl Iodides with (Difluoromethyl)zinc Reagent

Serizawa, Hiroki,Ishii, Koki,Aikawa, Kohsuke,Mikami, Koichi

supporting information, p. 3686 - 3689 (2016/08/16)

The combination of difluoroiodomethane and zinc dust or diethylzinc can readily lead to (difluoromethyl)zinc reagents. Therefore, the first copper-catalyzed difluoromethylation of aryl iodides with the zinc reagents is accomplished to afford the difluorom

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1691-13-0