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61794-43-2

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61794-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61794-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,9 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61794-43:
(7*6)+(6*1)+(5*7)+(4*9)+(3*4)+(2*4)+(1*3)=142
142 % 10 = 2
So 61794-43-2 is a valid CAS Registry Number.

61794-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,5-tetrafluoro-3-iodo-6-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1,2,4,5-tetrafluoro-3-iodo-6-(trifluoromethyl)

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:61794-43-2 SDS

61794-43-2Relevant articles and documents

A versatile and highly reactive polyfluorinated hypervalent iodine (III) compound

Schaefer, Sascha,Wirth, Thomas

experimental part, p. 2786 - 2789 (2010/07/06)

(Figure Presented) Hyper-reactive: A highly reactive, fully fluorinated hypervalent iodine reagent (see formula) mediates new transformations (e.g. the one-pot conversion of sulfides to sulfoximines) and serves as a stoichiometric oxidant in well-established reactions (e.g. C-C bond cleavage and the conversion of alcohols into aldehydes).

REACTIONS OF POLYFLUOROARYL BROMIDES AND IODIDES WITH C-, Si-, Ge-, Sn- AND Pb-ELECTROPHILES AND TRIS(DIALKYLAMINO)PHOSPHINES

Bardin, V. V.,Pressman, L. S.,Rogoza, L. N.,Furin, G. G.

, p. 213 - 231 (2007/10/02)

The reactions of polyfluoroaryl bromides ArFBr or iodides ArFI with P(NR'2)3 and R3MX (R = alkyl; M = Si, Ge, Sn and Pb; X = Cl, Br) led to the formation of ArFMR3.The reactions of C6F5Br with P(NEt2)3 and C-electrophiles (CH3I, C6F5CF3 and (CF3)2C=CFC2F5) gave the products of pentafluorophenylation of these substrates.

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