Welcome to LookChem.com Sign In|Join Free

CAS

  • or

678-77-3

Post Buying Request

678-77-3 Suppliers

Recommended suppliersmore

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

678-77-3 Usage

Uses

Hexafluoroglutaryl Chloride (CAS# 678-77-3) can be used to treat VOCs waste gas. It can also be used to prepare triptyl polymer separating membrane.

Check Digit Verification of cas no

The CAS Registry Mumber 678-77-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 678-77:
(5*6)+(4*7)+(3*8)+(2*7)+(1*7)=103
103 % 10 = 3
So 678-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C5Cl2F6O2/c6-1(14)3(8,9)5(12,13)4(10,11)2(7)15

678-77-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A14200)  Hexafluoroglutaryl chloride, 97%   

  • 678-77-3

  • 1g

  • 202.0CNY

  • Detail
  • Alfa Aesar

  • (A14200)  Hexafluoroglutaryl chloride, 97%   

  • 678-77-3

  • 5g

  • 702.0CNY

  • Detail
  • Alfa Aesar

  • (A14200)  Hexafluoroglutaryl chloride, 97%   

  • 678-77-3

  • 25g

  • 2675.0CNY

  • Detail

678-77-3SDS

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 Hexafluoroglutaryl chloride

1.2 Other means of identification

Product number -
Other names 2,2,3,3,4,4-hexafluoropentanedioyl dichloride

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:678-77-3 SDS

678-77-3Relevant articles and documents

Method for preparing fluorine-containing dihydric alcohol from fluorine-containing cycloolefin

-

Paragraph 0046, (2021/07/01)

The invention discloses a method for preparing fluorine-containing dihydric alcohol from fluorine-containing cycloolefin. The method comprises the following steps: oxidizing fluorine-containing cycloolefin serving as a raw material by using an oxidizing agent and treating the fluorine-containing cycloolefin by using a strong alkali to generate a solid mixed salt containing corresponding fluorine-containing dicarboxylate, and then generating corresponding fluorine-containing binary acyl chloride under the action of an acylating chlorination reagent; and finally, enabling the fluorine-containing binary acyl chloride and a reducing agent to be subjected to a reduction reaction under the action of a solvent and a catalyst to obtain the corresponding fluorine-containing dihydric alcohol. The specific organic solvent and catalyst are adopted, and other conditions are matched, so that the fluorine-containing cycloolefin can be effectively promoted to generate corresponding fluorine-containing dihydric alcohol with high efficiency and high yield. The method has the advantages of easily available raw materials, simple process, convenience in operation, low cost and the like, and is suitable for large-scale production of fluorine-containing dihydric alcohol.

METHODS OF MAKING POLYFUNCTIONAL POLYFLUORINATED COMPOUNDS

-

, (2019/07/13)

A method of making a polyfunctional polyfluorinated compound includes combining first components that include a polyfluorinated cyclic compound having 4 to 7 ring carbon atoms and at least one of osmium tetroxide, ruthenium tetroxide or a precursor thereof and forming a polyfluorinated dicarboxylic acid. Two of the ring carbon atoms of the polyfluorinated cyclic compound form a double bond or an epoxide. The precursor reacts with an oxidant to form ruthenium tetroxide. Methods also include converting the polyfluorinated dicarboxylic acid to a polyfluorinated dicarboxylic acid halide and converting the polyfluorinated dicarboxylic acid halide to other polyfunctional polyfluorinated compounds.

An ω-functionalized perfluoroalkyl chain: Synthesis and use in liquid crystal design

Pensec, Sandrine,Tournilhac, Francois-Genes

, p. 441 - 442 (2007/10/03)

A multiblock polyphilic compound incorporating a perfluoroalkyl spacer and associating groups at both extremities exhibits smectic A and smectic C mesophases.

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 678-77-3