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Stannane, dibromobis(pentafluorophenyl)-, also known as (pentafluorophenyl)dibromostannane, is a chemical compound with the molecular formula C12H2Br2F10Sn. It is a derivative of tin, characterized by the presence of two bromine atoms and two pentafluorophenyl groups attached to a central tin atom. This organotin compound is known for its unique electronic properties and potential applications in various fields, including organic synthesis, materials science, and as a precursor in the production of other organotin compounds. Due to its stability and reactivity, it is often used in the synthesis of complex organotin molecules and as a ligand in coordination chemistry.

5375-99-5

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5375-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5375-99-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5375-99:
(6*5)+(5*3)+(4*7)+(3*5)+(2*9)+(1*9)=115
115 % 10 = 5
So 5375-99-5 is a valid CAS Registry Number.

5375-99-5SDS

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 dibromo-bis(2,3,4,5,6-pentafluorophenyl)stannane

1.2 Other means of identification

Product number -
Other names Stannane,dibromobis(pentafluorophenyl)

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:5375-99-5 SDS

5375-99-5Relevant academic research and scientific papers

Preparation, reactivities, and NMR spectra of pentafluorophenyltin derivatives

Chen, Jian-Xie,Sakamoto, Katsumasa,Orita, Akihiro,Otera, Junzo

, p. 58 - 65 (2007/10/03)

A variety of pentafluorophenyltin compounds were prepared and their chemical properties were examined. These compounds effectively catalyzed Mukaiyama-aldol reaction of ketene silyl acetal in sharp contrast to the inertness of normal alkyltin halides like Bu2SnCl2. The increased Lewis acidity of the pentafluorophenyltin halides was proved by 119Sn- and 13C-NMR spectra. On the other hand, the pentafluorophenyl group reduced the reactivities of tin towards both nucleophiles and electrophiles. 19F-NMR spectroscopy was invoked to elucidate this anomaly.

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