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17305-95-2

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17305-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17305-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,0 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17305-95:
(7*1)+(6*7)+(5*3)+(4*0)+(3*5)+(2*9)+(1*5)=102
102 % 10 = 2
So 17305-95-2 is a valid CAS Registry Number.

17305-95-2SDS

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 chloro(chloromethyl)mercury

1.2 Other means of identification

Product number -
Other names Chloromethylmercuric chloride

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:17305-95-2 SDS

17305-95-2Downstream Products

17305-95-2Relevant articles and documents

The vibrational spectra of chloromethyl mercuric chloride, ClCH2HgCl

Edwards, H. G. M.

, p. 427 - 430 (1986)

The Raman and IR spectra of ClCH2HgCl are reported for the firts time and a complete vibrational assignment is made on the basis of Cs symmetry.Force constant calculations based on an SVFF approximation indicate that the mercury-carbon stretching force constant is decreased by 30 percent on introduction of a chlorine atom into the methyl group of CH3HgCl.

Preparation of (Chloromethyl)palladium(II) Derivatives from Complexes of Palladium Dichloride by Reaction with Diazomethane or Bis(chloromethyl)-mercury

McCrindle, Robert,Arsenault, Gilles J.,Farwaha, Rajeev,McAlees, Alan J.,Sneddon, David W.

, p. 761 - 766 (2007/10/02)

Treatment, with diazomethane, of a range of palladium dichloride and dibromide complexes containing chelaing ligands has been examined.With all but one, the formation of a mono(halogenomethyl) product was observed.The methylene insertion products from complexes of palladium dichloride are relatively stable if at least one olefin or phosphine ligand is present, but with bis-amine or -sulphide ligands the insertion products could not be isolated.However, all of the insertion products showed at least some tendency to revert to the starting dichloro complexes by loss of the methylene moiety.Products of insertion into a Pd-Br bond are less readily formed than those of the corresponding chloride and the resulting bromomethyl derivatives are less stable than their chloromethyl analogues.Chloromethyl derivatives were also prepared from the dichloride by treatment with bis(chloromethyl)mercury (only one of the two chloromethyl groups is transfered) or from a performed chloromethyl complex by ligand exchange.

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