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27143-34-6

27143-34-6

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27143-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27143-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,4 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27143-34:
(7*2)+(6*7)+(5*1)+(4*4)+(3*3)+(2*3)+(1*4)=96
96 % 10 = 6
So 27143-34-6 is a valid CAS Registry Number.

27143-34-6SDS

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 (2-thiocyanatocyclohexyl) thiocyanate

1.2 Other means of identification

Product number -
Other names -

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:27143-34-6 SDS

27143-34-6Relevant articles and documents

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Bonnet,R. et al.

, p. 2439 - 2444 (1976)

-

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Dermer,Dysinger

, p. 750 (1939)

-

Radical additions to olefins in the presence of iodobenzenediacetate: An easy route to alkyl dithiocyanates

De Mico, Antonella,Margarita, Roberto,Mariani, Andrea,Piancatelli, Giovanni

, p. 1889 - 1892 (2007/10/03)

We describe a new application of iodobenzenediacetate (IBDA), which is able to oxidize thiocyanate anion to the corresponding radical. Subsequent addition to nucleophilic olefins leads to dithiocyanate derivatives. The radical addition to olefins is more effective when performing the thiocyanation reaction in presence of Mg(ClO4)2 or TEMPO.

KINETICS AND DOPING EFFECT IN THE ADDITION OF 2,4-DINITROPHENYLSULFENYL CHLORIDE AND DITHIOCYANOGEN TO OLEFINS

Skorobogatova, E. V.,Grudzinskaya, E. Yu.,Afanas'ev, P. S,Kartashov, V. R.,Zefirov, N. S.,Caple, R.

, p. 1814 - 1822 (2007/10/02)

The rate of the doping addition in the reactions of 2,4-dinitrophenylsulfenyl chloride with cyclohexene an methylenecyclobutane and of dithiocyanogen with cyclohexene and substituted styrenes in the presence of lithium perchlorate is described by the normal salt effect equation.On the other hand, the rate of formation of the doping products may exceed or lag behind the increase in the total reaction rate.These results were interpreted in the framework of an ion-pair mechanism.

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