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Trimethyl(2,2,3,3-tetrafluorocyclobutyl)silane is an organosilicon compound characterized by its unique structure and properties. It is composed of a cyclobutane ring with four fluorine atoms and a silicon atom bonded to three methyl groups. trimethyl(2,2,3,3-tetrafluorocyclobutyl)silane is known for its thermal stability and resistance to hydrolysis, making it a valuable intermediate in the synthesis of various fluorinated organic compounds and materials. Its applications span across different industries, including pharmaceuticals, agrochemicals, and specialty chemicals, where it is used to introduce fluorine-containing groups into target molecules. The compound's stability and reactivity are key factors in its utility, offering a platform for the development of new products with enhanced properties.

312-81-2

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312-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312-81-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 312-81:
(5*3)+(4*1)+(3*2)+(2*8)+(1*1)=42
42 % 10 = 2
So 312-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H12F4Si/c1-12(2,3)5-4-6(8,9)7(5,10)11/h5H,4H2,1-3H3

312-81-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-(2,2,3,3-tetrafluorocyclobutyl)silane

1.2 Other means of identification

Product number -
Other names 2.2.3.3-Tetrafluor-cyclobutyl-trimethylsilan

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:312-81-2 SDS

312-81-2Relevant academic research and scientific papers

2,3,3-Trifluoro-1-cyclobutene and Dimers of 1,1,2-Trifluoro-1,3-butadiene from Tetrafluoroethylene-Vinylsilane Cycloadducts

England, David C.,Weigert, Frank J.,Calabrese, Joseph C.

, p. 4816 - 4819 (2007/10/02)

(Tetrafluorocyclobutyl)silanes prepared by thermal cycloaddition of tetrafluoroethylene (TFE) to vinylsilanes were pyrolyzed at 600 deg C to give mixtures containing dimers of 1,1,2-trifluoro-1,3-butadiene.The monomeric diene 1 was undoubtly an intermediate formed by ring opening of initially formed 2,3,3-trifluoro-1-cyclobutene (9).This cyclobutene has been prepared by fluoride ion catalyzed removal of trimethylfluorosilane from (2,2,3,3-tetrafluorocyclobutyl)trimethylsilane (8) at room temperature.One of the dimers of the diene was saturated and was shown by X-raycrystallography to have the tricyclooctane structure (3) corresponding to a previously reported structure for a perfluorobutadiene dimer.The cyclooctadiene 2 presumed to be the precursor to dimer 3 and Diels-Alder dimers (vinylcyclohexenes) 4 and 7 were characterized by 19F NMR analyses of liquid fractions.

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