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Heptanamide, 2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoro-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

315237-99-1

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315237-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 315237-99-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,5,2,3 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 315237-99:
(8*3)+(7*1)+(6*5)+(5*2)+(4*3)+(3*7)+(2*9)+(1*9)=131
131 % 10 = 1
So 315237-99-1 is a valid CAS Registry Number.

315237-99-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoro-N-phenylheptanamide

1.2 Other means of identification

Product number -
Other names Heptanamide,2,2,3,3,4,4,5,5,6,6,7,7,7-tridecafluoro-N-phenyl

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:315237-99-1 SDS

315237-99-1Downstream Products

315237-99-1Relevant academic research and scientific papers

Perfluoroalkylation in flow microreactors: Generation of perfluoroalkyllithiums in the presence and absence of electrophiles

Nagaki, Aiichiro,Tokuoka, Shinya,Yamada, Shigeyuki,Tomida, Yutaka,Oshiro, Kojun,Amii, Hideki,Yoshida, Jun-Ichi

, p. 7559 - 7563 (2011)

Perfluoroalkyllithiums were effectively generated from perfluoroalkyl halides in the presence and absence of electrophiles using flow microreactor systems. The in situ trapping with electrophile is conducted at much higher temperatures than those required for batch macro reactors. The subsequent trapping method is quite effective for highly reactive electrophiles that are not compatible with the lithiation process.

Method for Producing Fluorine-Containing Substituted Compound and Fluorine-Containing Substituted Compound

-

Paragraph 0280-0282, (2014/02/15)

A method for producing a fluorine-containing substituted compound, the method including: introducing an organofluorine compound and an organolithium compound into a microreactor provided with a flow path capable of mixing a plurality of liquids, to thereby obtain a reaction product; and introducing, into the microreactor, the reaction product and an electrophile exhibiting electrophilic effect on the reaction product, to thereby obtain a fluorine-containing substituted compound.

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