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[4-(dimethylamino)phenyl]mercury acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23332-31-2

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23332-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23332-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,3 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23332-31:
(7*2)+(6*3)+(5*3)+(4*3)+(3*2)+(2*3)+(1*1)=72
72 % 10 = 2
So 23332-31-2 is a valid CAS Registry Number.

23332-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name acetyloxy-[4-(dimethylamino)phenyl]mercury

1.2 Other means of identification

Product number -
Other names p-dimethylaminophenylmercury acetate

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:23332-31-2 SDS

23332-31-2Relevant academic research and scientific papers

Characterisation of the first authenticated organomercury hydroxide, 4-Me2NC6H4HgOH

Nicholson, Brian K.,Whitley, Sam K.

, p. 515 - 521 (2007/10/03)

4-Me2NC6H4HgOH was prepared from 4-Me2NC6H4HgOAc. Full characterisation showed that it crystallises as discrete molecules, the first example of a true organomercury hydroxide in the solid state. The structures of 4-Me2NC6H4HgOAc and (4-Me2NC6H4)2Hg are also discussed.

Organocobalt Cluster Complexes. 23. Novel Chemistry of (Acylmethylidyne)- and (Aroylmethylidyne)tricobalt Nonacarbonyl Complexes

Seyferth, Dietmar,Nestle, Mara Ozolins

, p. 3320 - 3328 (2007/10/02)

(Acylmethylidyne)- and (aroylmethylidyne)tricobalt nonacarbonyl complexes undergo reduction with molecular hydrogen in refluxing benzene with no added catalyst at atmospheric pressure to produce the respective (α-hydroxyalkylidyne)tricobalt nonacarbonyls and , in some cases, the completely reduced alkylidynetricobalt nonacarbonyls.These tricobalt-carbon cluster-substituted ketones also undergo complete reduction to the corresponding alkylidynetricobalt nonacarbonyl when treated with tetrafluoroacetic acid in refluxing benzene. (Acylmethylidyne)- and (aroylmethylidyne)tricobalt nonacarbonyl complexes also were found to undergo facile thermal decarbonylation to yield the corresponding (alkylmethylidyne)- and (aroylmethylidyne)tricobalt nonacarbonyl complexes.These unusual reactions were attributed to the uniqueness of the C=O bond in these ketones, and a discussion of possible mechanisms is included.In addition, it was found that in refluxing benzene (α-hydroxyalkylidyne)tricobalt nonacarbonyl complexes revert to the respective ketone complexes.

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