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33094-27-8

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33094-27-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33094-27-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,9 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33094-27:
(7*3)+(6*3)+(5*0)+(4*9)+(3*4)+(2*2)+(1*7)=98
98 % 10 = 8
So 33094-27-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H36Cl2O2/c1-3-4-5-6-8-11-14-17(20)18(21)15-12-9-7-10-13-16-19(22)23-2/h17-18H,3-16H2,1-2H3

33094-27-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 9,10-dichlorooctadecanoate

1.2 Other means of identification

Product number -
Other names 9,10-dichlorostearic acid methyl ester

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:33094-27-8 SDS

33094-27-8Downstream Products

33094-27-8Relevant articles and documents

Electrocatalytic Radical Dichlorination of Alkenes with Nucleophilic Chlorine Sources

Fu, Niankai,Sauer, Gregory S.,Lin, Song

supporting information, p. 15548 - 15553 (2017/11/06)

We report a Mn-catalyzed electrochemical dichlorination of alkenes with MgCl2 as the chlorine source. This method provides operationally simple, sustainable, and efficient access to a variety of vicinally dichlorinated compounds. In particular, alkenes with oxidatively labile functional groups, such as alcohols, aldehydes, sulfides, and amines, were transformed into the desired vicinal dichlorides with high chemoselectivity. Mechanistic data are consistent with metal-mediated Cl atom transfer as the predominant pathway enabling dual C-Cl bond formation and contradict an alternative pathway involving electrochemical evolution of chlorine gas followed by Cl2-mediated electrophilic dichlorination.

Organic halogen compounds, EOX, in mussels from a clean lake and a pulp mill recipient

Pellinen, Jukka,Ruokolainen, Minna,Maekelae, Petteri,Taskinen, Jouni

, p. 1515 - 1526 (2007/10/03)

The extractable organic halogen (EOX) residue of duck mussels, Anodonta anatina, from the unpolluted Lake Hoytiainen, Finland, was found to be 690 μg/g of lipids. The residue was characterized by analyzing chlorinated phenols, hydrocarbons and fatty acids. These compound classes accounted only for 1.9% of the EOX. Mussels from the same lake were incubated in a lake receiving pulp and paper mill effluents for 12 months to study the bioaccumulation of organochlorine compounds. The EOX of these mussels was 2045 μg/g lipids and only 1.1% of the residue was explained by the low molecular weight compounds. Thus, the majority of EOX remains undefined. However, potential differences in composition are suggested by the relative proportion of defined compounds and the differences among the measured compound classes. These halogen compounds may be of natural origin or reaction products of anthropogenic compounds with humic substances. The presence of such compounds should be taken into account when evaluating the accumulation of pulp mill effluent-related EOX in mussels. No difference was found in the EOX between male and female mussels caged close to a pulp mill, but, on dry weight basis, mussels infected by a digenean parasite had higher EOX concentration than healthy females.

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