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56003-60-2

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56003-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56003-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,0 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56003-60:
(7*5)+(6*6)+(5*0)+(4*0)+(3*3)+(2*6)+(1*0)=92
92 % 10 = 2
So 56003-60-2 is a valid CAS Registry Number.

56003-60-2SDS

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 6-fluoro-4,4-dimethylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 6-fluoro-4,4-dimethylcyclohex-2-enone

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:56003-60-2 SDS

56003-60-2Relevant articles and documents

-

Desobry,V.,Margaretha,P.

, p. 2161 - 2163 (1975)

-

Micellar-system-mediated direct fluorination of ketones in water

Stavber, Gaj,Zupan, Marko,Stavber, Stojan

scheme or table, p. 589 - 594 (2009/07/09)

A micellar system was developed and applied for direct regioselective fluorination of a variety of cyclic and acyclic ketones to α-fluoroketones in water as reaction medium with Selectfluor F-TEDA-BF4 as fluorinating reagent. The inexpensive ionic amphiphile sodium dodecyl sulfate (SDS) was found to be an excellent promoter for fluorofunctionalization of hydrophobic ketones without prior activation or use of acid catalysts. Georg Thieme Verlag Stuttgart.

Direct α-fluorination of ketones using N-F reagents

Stavber, Stojan,Jereb, Marjan,Zupan, Marko

, p. 2609 - 2615 (2007/10/03)

The use of 1-fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Accufluor NFTh) as a fluorine atom transfer reagent and methanol as solvent enabled direct regiospecific fluorofunctionalization of the α-carbonyl position in ketones w

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