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Mercury bis(2-methylpropane-2-thiolate), also known as bis(2-methylpropane-2-thiolato)mercury, is a chemical compound with the formula Hg[S(CH(CH3)2]2. It is a coordination complex where mercury is the central metal atom, coordinated to two 2-methylpropane-2-thiolate ligands. mercury bis(2-methylpropane-2-thiolate) is a type of organomercury compound, which are known for their potential toxicity and environmental impact. It is characterized by its ability to form stable complexes with sulfur-containing ligands, which can influence its chemical reactivity and stability. Due to the presence of mercury, mercury bis(2-methylpropane-2-thiolate) is of interest in studies related to heavy metal pollution and the development of methods for its detection and remediation.

3374-16-1

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3374-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3374-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3374-16:
(6*3)+(5*3)+(4*7)+(3*4)+(2*1)+(1*6)=81
81 % 10 = 1
So 3374-16-1 is a valid CAS Registry Number.

3374-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Bis(tert-butylthio)mercury

1.2 Other means of identification

Product number -
Other names di(tert-butylsulfenyl)mercury

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:3374-16-1 SDS

3374-16-1Downstream Products

3374-16-1Relevant academic research and scientific papers

Perfluoromethyl element ligands. XLI. [1] compounds of the type (F3C)2EE′R with pseudohalide character (E = P, As; E′ = S, Se, Te)

Grobe,Vetter

, p. 2085 - 2094 (2008/10/08)

Perfluoromethyl phosphorus and -arsenic compounds of the type (F3C)2EE′R (E = P, As; E′ = S, Se, Te; R = organic group) are prepared either by dismutation (metathesis) of E2(CF3)4 with (RE′)2/su

Synthesis of Thiol, Selenol, and Tellurol Esters by the Reaction of Organochalcogeno Mercurials with Acid Chlorides

Silveira, Claudio C.,Braga, Antonio L.,Larghi, Enrique L.

, p. 5183 - 5186 (2008/10/08)

Summary: Thiol, selenol, and tellurol esters were prepared by the reaction of bis(organochalcogeno)mercurials with acid chlorides in chloroform or carbon tetrachloride and in the presence of tetrabutylammonium halides as catalysts.

Syntheses and Vibrational Spectra of Some Tris(alkanethiolato)mercurate(II) Complexes, and Crystal Structure of the Hexakis-(methanethiolato)dimercurate(II) Dianion

Bowmaker, Graham A.,Dance, Ian G.,Dobson, Brian C.,Rogers, David Alan

, p. 1607 - 1618 (2007/10/02)

The complexes (R = Me, cation = Et4N+; R = But, cation = Et4N+, Bu4N+, +) have been prepared.The crystal structure of the methanethiolate complex shows that it contains centrosymmetric dinuclear anions 2- with distorted tetrahedral geometry about the mercury atoms.Vibrational spectroscopic evidence suggests that this complex dissociates on dissolution in ethanol to give mononuclear - species.The ButS- complexes appear to exist as mononuclear t)3>- species both in the solid state and in solution.The metal-sulfur stretching frequencies are assigned for all of the complexes studied, and the vibrational spectra are discussed in terms of the structures of the complex anions involved.Crystal data for 2Hg2(SCH3)6: a 8.656(5), b 9.130(6), c 12.368(8) Angstroem; α 102.16(4), β 105.51(4), γ 105.29(4) deg; space group P, Z 1, R 0.034, Rw 0.042.

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