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56734-76-0

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56734-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56734-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,3 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56734-76:
(7*5)+(6*6)+(5*7)+(4*3)+(3*4)+(2*7)+(1*6)=150
150 % 10 = 0
So 56734-76-0 is a valid CAS Registry Number.

56734-76-0SDS

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 2-(1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-Perfluorhexylcyclohexanon

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:56734-76-0 SDS

56734-76-0Downstream Products

56734-76-0Relevant articles and documents

A novel synthesis of α-(perfluoroalkyl) ketones

Hu, Chang-Ming,Tang, Xiao-Qing,Qing, Feng-Ling

, p. 405 - 407 (2007/10/02)

Reaction of sodium perhalofluoroalkyl sulfinates with alkenes under UV irradiation and oxygen atmosphere provides α-perhalofluoroalkyl ketones in good yields.

TRIETHYLBORANE INDUCED PERFLUOROALKYLATION OF SILYL ENOL ETHERS OR GERMYL ENOL ETHERS WITH PERFLUOROALKYL IODIDES

Miura, Katsukiyo,Taniguchi, Masahiko,Nozaki, Kyoko,Oshima, Koichiro,Utimoto, Kiitiro

, p. 6391 - 6394 (2007/10/02)

Reaction of perfluoralkyl iodides with silyl enol ethers mediated by Et3B in the presence of a base provides perfluoroalkylated silyl enol ethers.Meanwhile, treatment of germyl enol ethers with perfluoroalkyl iodides affords α-perfluoroalkyl ketones in good yields.

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