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Triphenylstibane-trifluoroacetic acid (1:2) is a chemical mixture consisting of triphenylstibane and trifluoroacetic acid in a 1:2 ratio. Triphenylstibane, with the chemical formula (C6H5)3Sb, is an organostibine compound featuring three phenyl groups attached to a central antimony atom. Trifluoroacetic acid, on the other hand, has the chemical formula CF3COOH and is a colorless, corrosive liquid with strong acidic properties. This mixture is utilized in various chemical reactions and processes, taking advantage of the unique properties of both components. The combination of triphenylstibane's organometallic nature and trifluoroacetic acid's acidity can lead to interesting chemical transformations and applications in the fields of organic synthesis and materials science.

36971-66-1

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36971-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36971-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,7 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36971-66:
(7*3)+(6*6)+(5*9)+(4*7)+(3*1)+(2*6)+(1*6)=151
151 % 10 = 1
So 36971-66-1 is a valid CAS Registry Number.

36971-66-1SDS

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 [triphenyl-(2,2,2-trifluoroacetyl)oxy-λ5-stibanyl] 2,2,2-trifluoroacetate

1.2 Other means of identification

Product number -
Other names [triphenyl-(2,2,2-trifluoroacetyl)oxy-$l^{5}-stibanyl] 2,2,2-trifluoroacetate

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:36971-66-1 SDS

36971-66-1Relevant academic research and scientific papers

Pd-catalyzed C-arylation of unsaturated compounds with pentavalent triarylantimony dicarboxylates

Moiseev, Dmitry V.,Gushchin, Aleksey V.,Shavirin, Andrey S.,Kursky, Yury A.,Dodonov, Viktor A.

, p. 176 - 184 (2007/10/03)

Triarylantimony (V) derivatives Ar3SbX2 (X = Hal or acyloxy) were prepared by reaction of Ar3Sb with equimolar amounts of a peroxide ROOH (R = t-Bu, H) in the presence of an acid or an anhydride in good to excellent yields. Ar3Sb(O2CR)2 are mild and efficient C-arylation reagents of unsaturated compounds (methyl acrylate, styrene, 2-phenylpropene and acrylonitrile) under palladium catalysis at 50 °C, with PdCl2 being the most effective catalyst. Ar3SbHal2 do not react under these conditions.

Electrochemistry of hypervalent compounds - V. Anodic oxidation of trivalent organoantimony and organobismuth compounds

Fuchigami, Toshio,Miyazaki, Motoko

, p. 1979 - 1984 (2008/10/08)

Anodic oxidation of triphenylantimony in the presence of various oxygen nucleophiles or halide ions provided the corresponding hypervalent compounds having Sb - Y bonds (Y = RCOO, F, Cl, Br) in good yields. On the contrary, anodic oxidation of triphenylbi

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