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Stannane, [(dichloroacetyl)oxy]triphenyl-, also known as triphenyl(dichloroacetyloxy)stannane, is a chemical compound with the molecular formula C20H15Cl2O2Sn. It is a derivative of triphenylstannane, where one of the phenyl groups is replaced by a dichloroacetyloxy group. This organotin compound is characterized by its potential applications in various chemical reactions and processes, such as in the synthesis of other organotin compounds or as a reagent in organic synthesis. Due to its specific structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest in the field of organometallic chemistry.

7546-89-6

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7546-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7546-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7546-89:
(6*7)+(5*5)+(4*4)+(3*6)+(2*8)+(1*9)=126
126 % 10 = 6
So 7546-89-6 is a valid CAS Registry Number.

7546-89-6SDS

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 triphenylstannyl 2,2-dichloroacetate

1.2 Other means of identification

Product number -
Other names Triphenylzinndichloracetat

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:7546-89-6 SDS

7546-89-6Downstream Products

7546-89-6Relevant academic research and scientific papers

The β-effect with vinyl cations: Kinetic study of the protiodemetalation of silyl-, germyl-, and stannylalkynes

Dallaire, Carol,Brook, Michael A.

, p. 2332 - 2338 (2008/10/08)

The relative magnitude of the hyperconjugative stabilization of vinyl cations by adjacent C-M bonds (M = Si, Ge, Sn; the β-effect) has been examined by measuring the rate constants for the protonation and subsequent protiodemetalation of group 14 metalated (trimethylsilyl)-acetylenes (R3MC≡CSiMe3). The relative β-effect arising from the second-order rate constants Sn ? Ge > Si (maximum kM/kSi = 108, 5 × 102, 1, respectively) follows the same order as that reported for simple carbenium ions. The product ratio from the protonation of Ph3GeC≡CSiMe3 was found to be particularly sensitive to acid concentration and strength, leading to loss of Ph3Ge preferentially with weaker acids. With tin groups, the rate of destannylation decreased with increasing steric bulk, unlike the corresponding situation with silyl groups. The origins of both these observations may be attributed to nucleophilic interaction at the metal center during protonation.

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