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33756-42-2

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33756-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33756-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,5 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33756-42:
(7*3)+(6*3)+(5*7)+(4*5)+(3*6)+(2*4)+(1*2)=122
122 % 10 = 2
So 33756-42-2 is a valid CAS Registry Number.

33756-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tri-p-fluorophenylantimony(III)

1.2 Other means of identification

Product number -
Other names tris(4-fluorophenyl)stibine

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:33756-42-2 SDS

33756-42-2Relevant articles and documents

Triarylantimony(V) catecholates – Derivatives of 4,5-difluoro-3,6-di-tert-butyl-o-benzoquinone

Poddel'sky, Andrey I.,Smolyaninov, Ivan V.,Fukin, Georgy K.,Berberova, Nadezhda T.,Cherkasov, Vladimir K.,Abakumov, Gleb A.

, p. 1 - 6 (2016)

New triarylantimony(V) 4,5-difluoro-3,6-di-tert-butylcatecholates of (4,5-F2-3,6-Cat)SbAr3type, where Ar is p-fluorophenyl (1), p-chlorophenyl (2), phenyl (3), have been synthesized and characterized in details. The electrochemical p

Novel tetranuclear triarylantimony(v) complexes with (±)-mandelic acid ligands: Synthesis, characterization, in vitro cytotoxicity and DNA binding properties

Jiang, Jin,Yin, Handong,Wang, Fangli,Han, Zhong,Wang, Fei,Cheng, Shuang,Hong, Min

, p. 8563 - 8566 (2013/07/27)

Four novel tetranuclear organoantimony(v) complexes [R3SbL] 4, in which LH = (±)-mandelic acid and R = phenyl (1), 4-fluorophenyl (2), 3-fluorophenyl (3), 3,4,5-trifluorophenyl (4), were synthesized and characterized. The complexes displayed rapid, low micromolar in vitro cytotoxicity against a range of epithelial tumour cells and efficient CT-DNA binding.

Fourier-transform Raman and infrared spectra and normal coordinate analysis of the triphenyl compounds and their methyl-, methoxy- and fluoro-substituted derivatives of arsenic, antimony and bismuth

Ludwig,Dolny,Goetze

, p. 2363 - 2372 (2007/10/03)

The Fourier transform (FT)-Raman and infrared (IR) spectra of triphenyl-, perdeuterated triphenyl-, tris(2-methylphenyl)-, tris(3-methylphenyl)-, tris(2,4,6-trimethylphenyl)-, tris(2-methoxyphenyl)-, tris(3-methoxyphenyl)-, tris(3-fluorophenyl)- and tris(

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