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Trimethylstannanylium benzenethiolate is a chemical compound with the formula (CH3)3SnSPh, where "Sn" represents tin, "S" represents sulfur, and "Ph" represents the phenyl group (C6H5). It is an organotin compound, which is a type of organometallic compound that contains a carbon-to-metal bond. This specific compound features a trimethyltin group (three methyl groups attached to a tin atom) and a benzenethiolate group (a sulfur atom bonded to a benzene ring). Trimethylstannanylium benzenethiolate is known for its unique reactivity and is used in various chemical reactions, particularly in the synthesis of organotin compounds and as a catalyst in certain organic transformations. Its properties, such as its stability and reactivity, make it a valuable tool in the field of organometallic chemistry.

1007-27-8

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1007-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1007-27-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1007-27:
(6*1)+(5*0)+(4*0)+(3*7)+(2*2)+(1*7)=38
38 % 10 = 8
So 1007-27-8 is a valid CAS Registry Number.

1007-27-8SDS

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 trimethyl(phenylsulfanyl)stannane

1.2 Other means of identification

Product number -
Other names trimethyl(phenylthio)stannane

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:1007-27-8 SDS

1007-27-8Relevant academic research and scientific papers

Novel room light-induced disproportionation reaction of organo-ditin and -dilead compounds with organic dichalcogenides: An efficient salt-free route to organo-tin and -lead chalcogenides

Mirzaei, Farzad,Han, Li-Biao,Tanaka, Masato

, p. 657 - 658 (2007/10/03)

Disproportionation of organo-ditin and -dilead compounds (R3M)2 (M = Sn, Pb) with organic dichalcogenides (R'Z)2 (Z = S, Se, Te) is efficiently promoted by room light to produce the corresponding organo-tin and -lead chalc

Thioether complexes of tungsten hexacarbonyl

Lucas, C. Robert

, p. 1758 - 1763 (2007/10/02)

The preparation of a series of organic and organometallic thioethers R3MSR' (M = C,Si,Ge, or Sn) is reported.From these, several new compounds of type 1 are synthesized, some of which contain para-substituted aryl functions for R and R'.In hexane solution in the carbonyl streching region of the ir the uv there is evidence for a degree of multiple bonding, at least in the M - S - WW - CO portion of these molecules.Multiple bonding extending into aromatic R or R'is small or non-existent and cannot be assessed precisely because of spontaneous decomposition of the complexes.All the complexes undergo a thermally initiated decomposition, the case of which depends on the nature of R, R', and M.The unusual W(I) thiolate cis-2 is the termal decomposition product.

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