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20883-32-3

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20883-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20883-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,8 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20883-32:
(7*2)+(6*0)+(5*8)+(4*8)+(3*3)+(2*3)+(1*2)=103
103 % 10 = 3
So 20883-32-3 is a valid CAS Registry Number.

20883-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro-(2,4,6-trimethylphenyl)mercury

1.2 Other means of identification

Product number -
Other names Chlormercuri-mesitylen

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:20883-32-3 SDS

20883-32-3Relevant articles and documents

Crystal structures and chemical properties of dimesitylcadmium and dimesitylmercury

Hayashi, Mari,Bolte, Michael,Wagner, Matthias,Lerner, Hans-Wolfram

, p. 646 - 649 (2011)

Mesityllithium was used to synthesize dimesitylcadmium and dimesitylmercury from CdCl2 and HgCl2, respectively. X-ray- crystallographic data show that the group 12 metal compounds M[Mes]2 (M = Zn, Cd, Hg) are isomorphous (monoclinic, P21/n). The asymmetric unit of M[Mes]2 (M = Zn, Cd, Hg) consists of one mesityl group bonded to the metal atom, which is related to the second substituent by an inversion center. In addition we have investigated the reaction of BBr3 with M[Mes]2 (M = Cd, Hg) for our understanding of the reactivity of donor-free group 12 mesityl compounds. The reaction of M[Mes]2 (M = Cd, Hg) with an excess of BBr3 produces MesBBr2. UV-induced conversion of Hg[Mes]2 in benzene yielded quantitatively mesitylene and mercury whereas irradiation of a chloroform solution of Hg[Mes]2 for 1290 min (λmax = 510 nm) gave mesitylene, Hg[Mes]Cl, and HgCl2 in a ratio of 6:4:1. Slow concentration of the reaction solution led to the deposition of X-ray quality crystals of the addition compound of two Hg[Mes]Cl molecules and HgCl 2 (monoclinic space group P21/n).

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