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66793-27-9

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66793-27-9 Usage

Description

(Bromomethyl)pentafluorosulfur(VI) is a chemical compound characterized by a bromine atom connected to a methyl group, which is further attached to a central sulfur atom encircled by five fluorine atoms. (Bromomethyl)pentafluorosulfur(VI) is known for its high reactivity and its ability to participate in a broad spectrum of chemical reactions, making it a versatile reagent in organic synthesis.

Uses

Used in Organic Synthesis:
(Bromomethyl)pentafluorosulfur(VI) is used as a reagent for the introduction of a sulfonate group into organic molecules, which is crucial for the synthesis of various organic compounds with specific properties and functions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (Bromomethyl)pentafluorosulfur(VI) is utilized as a key intermediate in the synthesis of potential drug candidates. Its reactivity allows for the creation of novel molecular structures that could exhibit therapeutic effects.
Used in Material Science:
(Bromomethyl)pentafluorosulfur(VI) is also employed in the field of material science, where it contributes to the development of new materials with tailored properties. These materials can be used in a range of applications, from electronics to advanced functional materials for various industries.
Used in the Creation of Advanced Functional Materials:
(Bromomethyl)pentafluorosulfur(VI) is used as a building block in the design and synthesis of advanced functional materials. Its unique reactivity and the ability to form stable chemical bonds with a variety of elements make it a valuable component in the development of materials with specific characteristics, such as improved stability, reactivity, or selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 66793-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,9 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66793-27:
(7*6)+(6*6)+(5*7)+(4*9)+(3*3)+(2*2)+(1*7)=169
169 % 10 = 9
So 66793-27-9 is a valid CAS Registry Number.
InChI:InChI=1/CH2BrF5S/c2-1-8(3,4,5,6)7/h1H2

66793-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bromomethyl(pentafluoro)-λ<sup>6</sup>-sulfane

1.2 Other means of identification

Product number -
Other names Sulfur,(bromomethyl)pentafluoro-,(OC-6-21)

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:66793-27-9 SDS

66793-27-9Downstream Products

66793-27-9Relevant articles and documents

Methylenesulfurtetrafluoride, CH2=SF4, Formation, Structure, and Chemistry

Kleemann, Gert,Seppelt, Konrad

, p. 645 - 658 (2007/10/02)

The preparation of methylenesulfurtetrafluoride, CH2=SF4, is achieved by bromine-lithium exchange on Br-CH2-SF5 at low temperatures and subsequent lithium fluoride elimination.CH2=SF4 is a colourless gas with b.p. -19 deg C and m.p. -139 deg C.The structure is essentially trigonal-bipyramidal, the methylene group occupying an equatorial position.The protons lie in the plane of the axial fluorine atoms.The molecule is rigid.The carbon-sulfur bond is best described as strong double bond with only little ylidic polarity. - The double bond undergoes numerous addition reactions with polar species under formation of cis-configurated X-CH2-SF4-Y systems.Less often elimination of SF4 and formation of carbene is observed.

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