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DIISOPROPYL-(1H,1H,2H,2H-PERFLUOROOCTYL)SILANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

356056-14-9

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356056-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 356056-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,6,0,5 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 356056-14:
(8*3)+(7*5)+(6*6)+(5*0)+(4*5)+(3*6)+(2*1)+(1*4)=139
139 % 10 = 9
So 356056-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H19F13Si/c1-7(2)28(8(3)4)6-5-9(15,16)10(17,18)11(19,20)12(21,22)13(23,24)14(25,26)27/h7-8,28H,5-6H2,1-4H3

356056-14-9 Well-known Company Product Price

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  • Aldrich

  • (00454)  Diisopropyl(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane  ≥95%

  • 356056-14-9

  • 00454-1G-F

  • 1,030.77CNY

  • Detail
  • Aldrich

  • (00454)  Diisopropyl(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane  ≥95%

  • 356056-14-9

  • 00454-5G-F

  • 4,126.59CNY

  • Detail

356056-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name di(propan-2-yl)-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane

1.2 Other means of identification

Product number -
Other names diisopropyl(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)silane

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:356056-14-9 SDS

356056-14-9Relevant academic research and scientific papers

Reaction and separation methods

-

, (2008/06/13)

A method of separating compounds that includes the steps of: tagging at least a first organic compound with a first tagging moiety to result in a first tagged compound; tagging at least a second organic compound with a second tagging moiety different from

Quasiracemic synthesis: Concepts and implementation with a fluorous tagging strategy to make both enantiomers of pyridovericin and mappicine

Zhang, Qisheng,Rivkin, Alexey,Curran, Dennis P.

, p. 5774 - 5781 (2007/10/03)

The concept of quasiracemic synthesis is introduced and illustrated with syntheses of both enantiomers of pyridovericin (whose absolute configuration is assigned as R) and mappicine. Like racemic synthesis, quasiracemic synthesis provides both enantiomers in a single synthetic sequence; however, separation tagging is used to ensure that quasiracemic mixtures can be analyzed, separated, and identified on demand. Fluorous tags of differing chain lengths are used to tag two enantiomeric starting materials. The resulting quasienantiomers are mixed to make a quasiracemate, which is then treated like a true racemate in successive steps of the synthesis. Fluorous chromatography is used to separate, or demix, the final quasiracemate into its two components, which are then detagged to provide (true) enantiomeric products. Quasiracemic synthesis is portrayed as the first and simplest of a series of mixture synthesis techniques based on separation tagging, and the prospects for using other types of separation tags are briefly evaluated.

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