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41424-33-3

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41424-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41424-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,2 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41424-33:
(7*4)+(6*1)+(5*4)+(4*2)+(3*4)+(2*3)+(1*3)=83
83 % 10 = 3
So 41424-33-3 is a valid CAS Registry Number.

41424-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name p-MeOC6H4(CF=CFCF3)

1.2 Other means of identification

Product number -
Other names 1-Methoxy-4-((Z)-pentafluoro-propenyl)-benzene

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:41424-33-3 SDS

41424-33-3Relevant articles and documents

Pentafluoropropenyl complexes of mercury, germanium, tin, and lead derived from (Z)-CFH=CFCF3 and their use as transfer reagents

Brisdon, Alan K.,Pritchard, Robin G.,Thomas, Anthony

experimental part, p. 1341 - 1348 (2012/04/10)

A series of new (E)-pentafluoropropenyl complexes of Hg, Ge, Sn, and Pb are reported derived from CFH=CFCF3 ((Z)-HFC-1225ye). Unequivocal assignment of the geometry of the products was achieved via a multinuclear (1H, 13C, 19F, 119Sn, and 199Hg) NMR study. These conclusions are confirmed in the single-crystal X-ray structures of Ph3Ge(CF=CFCF3) and Ph3Sn(CF=CFCF3). In the solid-state structures of both molecules, short contacts are observed between one of the fluorine atoms of the CF3 group and the metal center. The Bu3Sn(CF=CFCF 3) compound acts as an effective source of the pentafluoropropenyl group in a series of palladium-catalyzed Stille-Liebeskind reactions to generate new aryl-pentafluoropropenyl systems.

An Improved Synthesis of 1-Phenylpentafluoropropenes

Dmowski, Wojciech

, p. 25 - 30 (2007/10/02)

1-Phenylpentafluoropropene and a number of its para- and ortho-substituted derivatives were prepared in high yields by reaction of hexafluoropropene with etheral solutions of corresponding phenylmagnesium bromides in sealed glass tubes under autogenous pressure.The products were obtained as mixtures of the Z and E isomers, which ratios varied from 1/2 to 1/6 in favour of the E forms. 19F n.m.r. and i.r. spectra and b.p. of the 1-phenylpentafluoropropenes are reported.

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