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1800-91-5

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1800-91-5 Usage

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 1800-91-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,0 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1800-91:
(6*1)+(5*8)+(4*0)+(3*0)+(2*9)+(1*1)=65
65 % 10 = 5
So 1800-91-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H6F12/c1-3-5(11,12)7(15,16)9(19,20)10(21,22)8(17,18)6(13,14)4-2/h3-4H,1-2H2

1800-91-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-Divinylperfluorohexane

1.2 Other means of identification

Product number -
Other names 3,3,4,4,5,5,6,6,7,7,8,8-dodecafluorodeca-1,9-diene

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:1800-91-5 SDS

1800-91-5Relevant articles and documents

Fluorine-containing aromatic compound (by machine translation)

-

Paragraph 0032; 0047, (2017/04/07)

PROBLEM TO BE SOLVED: can be used as a crosslinking agent to provide new fluorine-containing aromatic compound. SOLUTION: compound eq. (1). With respect to the compound as a fluoroelastomer 100g, 0.5-30mmol, pref. 1-15mmol, more preferably 2.5-8mmol 1.5-13mmol further use of the crosslinking agent is preferably added. The larger the amount of additive, microaerobic wettabilit, the tendency of the improved heat resistance, and too excessively hardened linked product is obtained. Effect: fluoro-elastomer, can be used as a crosslinking agent, a crosslinking the compound obtained by the fluoro-elastomer, can be used as a sealing material, such as a seal ring or gasket which can be used in the molding. Selected drawing: no (by machine translation)

Synthesis of Fluorinated Acetylenes

Baum, Kurt,Bedford, Clifford D.,Hunadi, Ronald J.

, p. 2251 - 2257 (2007/10/02)

New routes to fluorinated acetylenes were developed on the basis of additions of iodofluorocarbons to silylacetylenes.Free radical addition of α,ω-diiodoperfluoroalkanes to (trimethylsilyl)acetylene gave the iodotrimethylsilyl olefins Me3SiIC=CH(CF2)nCH=CISiMe3, which reacted with potassium tert-butoxide or DBU to give the (trimethylsilyl)acetylenes and, with an excess of the base, the free diacetylenes.Perfluoroalkyl iodides similarly gave (perfluoroalkyl)acetylenes.The addition of perfluoroheptyl iodide to phenylacetylene, followed by treatment with potassium tert-butoxide gave 1-phenylperfluorononyne.The peroxide-catalyzed reactionof perfluoroalkyl iodides and bis(trimethylsilyl)acetylene gave 1:1 adducts, RF(Me2SiCH2I)C=CHSiMe3, resulting from intramolecular hydrogen abstraction by the initially formed vinyl radical.However, the thermal reaction of perfluoroalkyl iodides and diiodides with bis(trimethylsilyl)acetylene in the presence of free iodine gave the (trimethylsilyl)acetylenes, which were desilylated with potassium fluoride.A route to diacetylenes was investigated on the basis of addition of perfluoroiodo compounds to ethylene, dehydroiodination, brominations, and eliminations.

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