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54387-09-6

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54387-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54387-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,8 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54387-09:
(7*5)+(6*4)+(5*3)+(4*8)+(3*7)+(2*0)+(1*9)=136
136 % 10 = 6
So 54387-09-6 is a valid CAS Registry Number.

54387-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5-pentafluoro-6-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,pentafluoro(heptadecafluorooctyl)

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:54387-09-6 SDS

54387-09-6Relevant articles and documents

Perfluoroalkylations and perfluorooxaalkylations. Part 3. Chloro-substituted diazines as substrates in copper-mediated cross-coupling

Chen, Grace J.,Chen, Loomis S.

, p. 113 - 120 (2007/10/02)

The (perfluoroalkyl)- and (perfluorooxaalkyl)diazines, 2,4-bis(perfluorooctyl)pyrimidine (3), 2,4,6-tris(perfluorooctyl)pyrimidine (6a), 2,4,6-tris(perfluoro-6-methyl-5-oxaheptyl)pyrimidine (6b), 3,6-bis(perfluorooctyl)pyridazine (10) and 2,6-bis(perfluorooctyl)pyrazine (13), have been prepared in good yield.This was accomplished by using chloro-substituted diazines as substrates in copper mediated cross-coupling reactions with perfluoroalkyl and perfluorooxaalkyl iodides.The yields of the cross-coupled products are influenced by the reaction conditions as well as by the structure of the fluoroaliphatic iodides and substrates. - Keywords: Perfluoroalkylations; Perfluorooxaalkylations; Chloro-substituted diazines; Cross-coupling; NMR spectroscopy; Mass spectrometry

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